Novel compounds

ABSTRACT

Polypeptides and polynucleotides of the genes set forth in Table I and methods for producing such polypeptides by recombinant techniques are disclosed. Also disclosed are methods for utilizing polypeptides and polynucleotides of the genes set forth in Table I in diagnostic assays.

FIELD OF INVENTION

[0001] This invention relates to newly identified polypeptides and polynucleotides encoding such polypeptides, to their use in diagnosis and in identifying compounds that may be agonists, antagonists that are potentially useful in therapy, and to production of such polypeptides and polynucleotides. The polynucleotides and polypeptides of the present invention also relate to proteins with signal sequences which allow them to be secreted extracellularly or membrane-associated (hereinafter often referred collectively as secreted proteins or secreted polypeptides).

BACKGROUND OF THE INVENTION

[0002] The drug discovery process is currently undergoing a fundamental revolution as it embraces “functional genomics”, that is, high throughput genome- or gene-based biology. This approach as a means to identify genes and gene products as therapeutic targets is rapidly superseding earlier approaches based on “positional cloning”. A phenotype, that is a biological function or genetic disease, would be identified and this would then be tracked back to the responsible gene, based on its genetic map position.

[0003] Functional genomics relies heavily on high-throughput DNA sequencing technologies and the various tools of bioinformatics to identify gene sequences of potential interest from the many molecular biology databases now available. There is a continuing need to identify and characterise further genes and their related polypeptides/proteins, as targets for drug discovery.

[0004] Proteins and polypeptides that are naturally secreted into blood, lymph and other body fluids, or secreted into the cellular membrane are of primary interest for pharmaceutical research and development. The reason for this interest is the relative ease to target protein therapeutics into their place of action (body fluids or the cellular membrane). The natural pathway for protein secretion into extracellular space is the endoplasmic reticulum in eukaryotes and the inner membrane in prokaryotes (Palade, 1975, Science, 189, 347; Milstein, Brownlee, Harrison, and Mathews, 1972, Nature New Biol., 239, 117; Blobel, and Dobberstein, 1975, J. Cell. Biol., 67, 835). On the other hand, there is no known natural pathway for exporting a protein from the exterior of the cells into the cytosol (with the exception of pinocytosis, a mechanism of snake venom toxin intrusion into cells). Therefore targeting protein therapeutics into cells poses extreme difficulties.

[0005] The secreted and membrane-associated proteins include but are not limited to all peptide hormones and their receptors (including but not limited to insulin, growth hormones, chemokines, cytokines, neuropeptides, integrins, kallikreins, lamins, melanins, natriuretic hormones, neuropsin, neurotropins, pituitiary hormones, pleiotropins, prostaglandins, secretogranins, selectins, thromboglobulins, thymosins), the breast and colon cancer gene products, leptin, the obesity gene protein and its receptors, serum albumin, superoxide dismutase, spliceosome proteins, 7TM (transmembrane) proteins also called as G-protein coupled receptors, immunoglobulins, several families of serine proteinases (including but not limited to proteins of the blood coagulation cascade, digestive enzymes), deoxyribonuclease I, etc.

[0006] Therapeutics based on secreted or membrane-associated proteins approved by FDA or foreign agencies include but are not limited to insulin, glucagon, growth hormone, chorionic gonadotropin, follicle stimulating hormone, luteinizing hormone, calcitonin, adrenocorticotropic hormone (ACTh), vasopressin, interleukines, interferones, immunoglobulins, lactoferrin (diverse products marketed by several companies), tissue-type plasminogen activator (Alteplase by Genentech), hyaulorindase (Wydase by Wyeth-Ayerst), dornase alpha (Pulmozyme\ by Genentech), Chymodiactin (chymopapain by Knoll), alglucerase (Ceredase by Genzyme), streptokinase (Kabikinase by Pharmacia) (Streptase by Astra), etc. This indicates that secreted and membrane-associated proteins have an established, proven history as therapeutic targets. Clearly, there is a need for identification and characterization of further secreted and membrane-associated proteins which can play a role in preventing, ameliorating or correcting dysfunction or disease, including but not limited to diabetes, breast-, prostate-, colon cancer and other malignant tumors, hyper- and hypotension, obesity, bulimia, anorexia, growth abnormalities, asthma, manic depression, dementia, delirium, mental retardation, Huntington's disease, Tourette's syndrome, schizophrenia, growth, mental or sexual development disorders, and dysfunctions of the blood cascade system including those leading to stroke. The proteins of the present invention which include the signal sequences are also useful to further elucidate the mechanism of protein transport which at present is not entirely understood, and thus can be used as research tools.

SUMMARY OF THE INVENTION

[0007] The present invention relates to particular polypeptides and polynucleotides of the genes set forth in Table I, including recombinant materials and methods for their production. Such polypeptides and polynucleotides are of interest in relation to methods of treatment of certain diseases, including, but not limited to, the diseases set forth in Tables III and V, hereinafter referred to as “diseases of the invention”. In a further aspect, the invention relates to methods for identifying agonists and antagonists (e.g., inhibitors) using the materials provided by the invention, and treating conditions associated with imbalance of polypeptides and/or polynucleotides of the genes set forth in Table I with the identified compounds. In still a further aspect, the invention relates to diagnostic assays for detecting diseases associated with inappropriate activity or levels the genes set forth in Table I. Another aspect of the invention concerns a polynucleotide comprising any of the nucleotide sequences set forth in the Sequence Listing and a polypeptide comprising a polypeptide encoded by the nucleotide sequence. In another aspect, the invention relates to a polypeptide comprising any of the polypeptide sequences set forth in the Sequence Listing and recombinant materials and methods for their production. Another aspect of the invention relates to methods for using such polypeptides and polynucleotides. Such uses include the treatment of diseases, abnormalities and disorders (hereinafter simply referred to as diseases) caused by abnormal expression, production, function and or metabolism of the genes of this invention, and such diseases are readily apparent by those skilled in the art from the homology to other proteins disclosed for each attached sequence. In still another aspect, the invention relates to methods to identify agonists and antagonists using the materials provided by the invention, and treating conditions associated with the imbalance with the identified compounds. Yet another aspect of the invention relates to diagnostic assays for detecting diseases associated with inappropriate activity or levels of the secreted proteins of the present invention.

DESCRIPTION OF THE INVENTION

[0008] In a first aspect, the present invention relates to polypeptides the genes set forth in Table I. Such polypeptides include:

[0009] (a) an isolated polypeptide encoded by a polynucleotide comprising a sequence set forth in the Sequence Listing, herein when referring to polynucleotides or polypeptides of the Sequence Listing, a reference is also made to the Sequence Listing referred to in the Sequence Listing;

[0010] (b) an isolated polypeptide comprising a polypeptide sequence having at least 95%, 96%, 97%, 98%, or 99% identity to a polypeptide sequence set forth in the Sequence Listing;

[0011] (c) an isolated polypeptide comprising a polypeptide sequence set forth in the Sequence Listing;

[0012] (d) an isolated polypeptide having at least 95%, 96%, 97%, 98%, or 99% identity to a polypeptide sequence set forth in the Sequence Listing;

[0013] (e) a polypeptide sequence set forth in the Sequence Listing; and

[0014] (f) an isolated polypeptide having or comprising a polypeptide sequence that has an Identity Index of 0.95, 0.96, 0.97, 0.98, or 0.99 compared to a polypeptide sequence set forth in the Sequence Listing;

[0015] (g) fragments and variants of such polypeptides in (a) to (f).

[0016] Polypeptides of the present invention are believed to be members of the gene families set forth in Table II. They are therefore of therapeutic and diagnostic interest for the reasons set forth in Tables m and V. The biological properties of the polypeptides and polynucleotides of the genes set forth in Table I are hereinafter referred to as “the biological activity” of polypeptides and polynucleotides of the genes set forth in Table I. Preferably, a polypeptide of the present invention exhibits at least one biological activity of the genes set forth in Table I.

[0017] Polypeptides of the present invention also include variants of the aforementioned polypeptides, including all allelic forms and splice variants. Such polypeptides vary from the reference polypeptide by insertions, deletions, and substitutions that may be conservative or non-conservative, or any combination thereof. Particularly preferred variants are those in which several, for instance from 50 to 30, from 30 to 20, from 20 to 10, from 10 to 5, from 5 to 3, from 3 to 2, from 2 to 1 or 1 amino acids are inserted, substituted, or deleted, in any combination.

[0018] Preferred fragments of polypeptides of the present invention include an isolated polypeptide comprising an amino acid sequence having at least 30, 50 or 100 contiguous amino acids from an amino acid sequence set forth in the Sequence Listing, or an isolated polypeptide comprising an amino acid sequence having at least 30, 50 or 100 contiguous amino acids truncated or deleted from an amino acid sequence set forth in the Sequence Listing. Preferred fragments are biologically active fragments that mediate the biological activity of polypeptides and polynucleotides of the genes set forth in Table I, including those with a similar activity or an improved activity, or with a decreased undesirable activity. Also preferred are those fragments that are antigenic or immunogenic in an animal, especially in a human.

[0019] Fragments of a polypeptide of the invention may be employed for producing the corresponding full-length polypeptide by peptide synthesis; therefore, these variants may be employed as intermediates for producing the full-length polypeptides of the invention. A polypeptide of the present invention may be in the form of the “mature” protein or may be a part of a larger protein such as a precursor or a fusion protein. It is often advantageous to include an additional amino acid sequence that contains secretory or leader sequences, pro-sequences, sequences that aid in purification, for instance multiple histidine residues, or an additional sequence for stability during recombinant production.

[0020] Polypeptides of the present invention can be prepared in any suitable manner, for instance by isolation form naturally occurring sources, from genetically engineered host cells comprising expression systems (vide infra) or by chemical synthesis, using for instance automated peptide synthesizers, or a combination of such methods. Means for preparing such polypeptides are well understood in the art. In a further aspect, the present invention relates to polynucleotides of the genes set forth in Table I. Such polynucleotides include:

[0021] (a) an isolated polynucleotide comprising a polynucleotide sequence having at least 95%, 96%, 97%, 98%, or 99% identity to a polynucleotide sequence set forth in the Sequence Listing;

[0022] (b) an isolated polynucleotide comprising a polynucleotide set forth in the Sequence Listing;

[0023] (c) an isolated polynucleotide having at least 95%, 96%, 97%, 98%, or 99% identity to a polynucleotide set forth in the Sequence Listing;

[0024] (d) an isolated polynucleotide set forth in the Sequence Listing;

[0025] (e) an isolated polynucleotide comprising a polynucleotide sequence encoding a polypeptide sequence having at least 95%, 96%, 97%, 98%, or 99% identity to a polypeptide sequence set forth in the Sequence Listing;

[0026] (f) an isolated polynucleotide comprising a polynucleotide sequence encoding a polypeptide set forth in the Sequence Listing;

[0027] (g) an isolated polynucleotide having a polynucleotide sequence encoding a polypeptide sequence having at least 95%, 96%, 97%, 98%, or 99% identity to a polypeptide sequence set forth in the Sequence Listing;

[0028] (h) an isolated polynucleotide encoding a polypeptide set forth in the Sequence Listing;

[0029] (i) an isolated polynucleotide having or comprising a polynucleotide sequence that has an Identity Index of 0.95, 0.96, 0.97, 0.98, or 0.99 compared to a polynucleotide sequence set forth in the Sequence Listing;

[0030] (j) an isolated polynucleotide having or comprising a polynucleotide sequence encoding a polypeptide sequence that has an Identity Index of 0.95, 0.96, 0.97, 0.98, or 0.99 compared to a polypeptide sequence set forth in the Sequence Listing; and polynucleotides that are fragments and variants of the above mentioned polynucleotides or that are complementary to above mentioned polynucleotides, over the entire length thereof.

[0031] Preferred fragments of polynucleotides of the present invention include an isolated polynucleotide comprising an nucleotide sequence having at least 15, 30, 50 or 100 contiguous nucleotides from a sequence set forth in the Sequence Listing, or an isolated polynucleotide comprising a sequence having at least 30, 50 or 100 contiguous nucleotides truncated or deleted from a sequence set forth in the Sequence Listing.

[0032] Preferred variants of polynucleotides of the present invention include splice variants, allelic variants, and polymorphisms, including polynucleotides having one or more single nucleotide polymorphisms (SNPs).

[0033] Polynucleotides of the present invention also include polynucleotides encoding polypeptide variants that comprise an amino acid sequence set forth in the Sequence Listing and in which several, for instance from 50 to 30, from 30 to 20, from 20 to 10, from 10 to 5, from 5 to 3, from 3 to 2, from 2 to 1 or 1 amino acid residues are substituted, deleted or added, in any combination.

[0034] In a further aspect, the present invention provides polynucleotides that are RNA transcripts of the DNA sequences of the present invention. Accordingly, there is provided an RNA polynucleotide that:

[0035] (a) comprises an RNA transcript of the DNA sequence encoding a polypeptide set forth in the Sequence Listing;

[0036] (b) is a RNA transcript of a DNA sequence encoding a polypeptide set forth in the Sequence Listing;

[0037] (c) comprises an RNA transcript of a DNA sequence set forth in the Sequence Listing; or

[0038] (d) is a RNA transcript of a DNA sequence set forth in the Sequence Listing;

[0039] and RNA polynucleotides that are complementary thereto.

[0040] The polynucleotide sequences set forth in the Sequence Listing show homology with the polynucleotide sequences set forth in Table II. A polynucleotide sequence set forth in the Sequence Listing is a cDNA sequence that encodes a polypeptide set forth in the Sequence Listing. A polynucleotide sequence encoding a polypeptide set forth in the Sequence Listing may be identical to a polypeptide encoding a sequence set forth in the Sequence Listing or it may be a sequence other than a sequence set forth in the Sequence Listing, which, as a result of the redundancy (degeneracy) of the genetic code, also encodes a polypeptide set forth in the Sequence Listing. A polypeptide of a sequence set forth in the Sequence Listing is related to other proteins of the gene families set forth in Table II, having homology and/or structural similarity with the polypeptides set forth in Table II. Preferred polypeptides and polynucleotides of the present invention are expected to have, inter alia, similar biological functions/properties to their homologous polypeptides and polynucleotides. Furthermore, preferred polypeptides and polynucleotides of the present invention have at least one activity of the genes set forth in Table I.

[0041] Polynucleotides of the present invention may be obtained using standard cloning and screening techniques from a cDNA library derived from mRNA from the tissues set forth in Table IV (see for instance, Sambrook et al., Molecular Cloning: A Laboratory Manual, 2nd Ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989)). Polynucleotides of the invention can also be obtained from natural sources such as genomic DNA libraries or can be synthesized using well known and commercially available techniques.

[0042] When polynucleotides of the present invention are used for the recombinant production of polypeptides of the present invention, the polynucleotide may include the coding sequence for the mature polypeptide, by itself, or the coding sequence for the mature polypeptide in reading frame with other coding sequences, such as those encoding a leader or secretory sequence, a pre-, or pro- or prepro-protein sequence, or other fusion peptide portions. For example, a marker sequence that facilitates purification of the fused polypeptide can be encoded. In certain preferred embodiments of this aspect of the invention, the marker sequence is a hexa-histidine peptide, as provided in the pQE vector (Qiagen, Inc.) and described in Gentz et al., Proc Natl Acad Sci USA (1989) 86:821-824, or is an HA tag. A polynucleotide may also contain non-coding 5′ and 3′ sequences, such as transcribed, non-translated sequences, splicing and polyadenylation signals, ribosome binding sites and sequences that stabilize mRNA.

[0043] Polynucleotides that are identical, or have sufficient identity to a polynucleotide sequence set forth in the Sequence Listing, may be used as hybridization probes for cDNA and genomic DNA or as primers for a nucleic acid amplification reaction (for instance, PCR). Such probes and primers may be used to isolate full-length cDNAs and genomic clones encoding polypeptides of the present invention and to isolate cDNA and genomic clones of other genes (including genes encoding paralogs from human sources and orthologs and paralogs from species other than ) that have a high sequence similarity to sequences set forth in the Sequence Listing, typically at least 95% identity. Preferred probes and primers will generally comprise at least 15 nucleotides, preferably, at least 30 nucleotides and may have at least 50, if not at least 100 nucleotides. Particularly preferred probes will have between 30 and 50 nucleotides. Particularly preferred primers will have between 20 and 25 nucleotides.

[0044] A polynucleotide encoding a polypeptide of the present invention, including homologs from species other than, may be obtained by a process comprising the steps of screening a library under stringent hybridization conditions with a labeled probe having a sequence set forth in the Sequence Listing or a fragment thereof, preferably of at least 15 nucleotides; and isolating full-length cDNA and genomic clones containing the polynucleotide sequence set forth in the Sequence Listing. Such hybridization techniques are well known to the skilled artisan. Preferred stringent hybridization conditions include overnight incubation at 42° C. in a solution comprising: 50% formamide, 5× SSC (150 mM NaCl, 15 mM trisodium citrate), 50 mM sodium phosphate (pH 7.6), 5×Denhardt's solution, 10 % dextran sulfate, and 20 microgram/ml denatured, sheared salmon sperm DNA; followed by washing the filters in 0.1× SSC at about 65° C. Thus the present invention also includes isolated polynucleotides, preferably with a nucleotide sequence of at least 100, obtained by screening a library under stringent hybridization conditions with a labeled probe having the sequence set forth in the Sequence Listing or a fragment thereof, preferably of at least 15 nucleotides.

[0045] The skilled artisan will appreciate that, in many cases, an isolated cDNA sequence will be incomplete, in that the region coding for the polypeptide does not extend all the way through to the 5′ terminus. This is a consequence of reverse transcriptase, an enzyme with inherently low “processivity” (a measure of the ability of the enzyme to remain attached to the template during the polymerisation reaction), failing to complete a DNA copy of the mRNA template during first strand cDNA synthesis.

[0046] There are several methods available and well known to those skilled in the art to obtain full-length cDNAs, or extend short cDNAs, for example those based on the method of Rapid Amplification of cDNA ends (RACE) (see, for example, Frohman et al., Proc Nat Acad Sci USA 85, 8998-9002, 1988). Recent modifications of the technique, exemplified by the Marathon (trade mark) technology (Clontech Laboratories Inc.) for example, have significantly simplified the search for longer cDNAs. In the Marathon (trade mark) technology, cDNAs have been prepared from mRNA extracted from a chosen tissue and an ‘adaptor’ sequence ligated onto each end. Nucleic acid amplification (PCR) is then carried out to amplify the “missing” 5′ end of the cDNA using a combination of gene specific and adaptor specific oligonucleotide primers. The PCR reaction is then repeated using ‘nested’ primers, that is, primers designed to anneal within the amplified product (typically an adapter specific primer that anneals further 3′ in the adaptor sequence and a gene specific primer that anneals further 5′ in the known gene sequence). The products of this reaction can then be analyzed by DNA sequencing and a full-length cDNA constructed either by joining the product directly to the existing cDNA to give a complete sequence, or carrying out a separate full-length PCR using the new sequence information for the design of the 5′ primer.

[0047] Recombinant polypeptides of the present invention may be prepared by processes well known in the art from genetically engineered host cells comprising expression systems. Accordingly, in a further aspect, the present invention relates to expression systems comprising a polynucleotide or polynucleotides of the present invention, to host cells which are genetically engineered with such expression systems and to the production of polypeptides of the invention by recombinant techniques. Cell-free translation systems can also be employed to produce such proteins using RNAs derived from the DNA constructs of the present invention.

[0048] For recombinant production, host cells can be genetically engineered to incorporate expression systems or portions thereof for polynucleotides of the present invention. Polynucleotides may be introduced into host cells by methods described in many standard laboratory manuals, such as Davis et al., Basic Methods in Molecular Biology (1986) and Sambrook et al.(ibid). Preferred methods of introducing polynucleotides into host cells include, for instance, calcium phosphate transfection, DEAE-dextran mediated transfection, transvection, micro-injection, cationic lipid-mediated transfection, electroporation, transduction, scrape loading, ballistic introduction or infection.

[0049] Representative examples of appropriate hosts include bacterial cells, such as Streptococci, Staphylococci, E. coli, Streptomyces and Bacillus subtilis cells; fungal cells, such as yeast cells and Aspergillus cells; insect cells such as Drosophila S2 and Spodoptera Sf9 cells; animal cells such as CHO, COS, HeLa, C127, 3T3, BHK, HEK 293 and Bowes melanoma cells; and plant cells.

[0050] A great variety of expression systems can be used, for instance, chromosomal, episomal and virus-derived systems, e.g., vectors derived from bacterial plasmids, from bacteriophage, from transposons, from yeast episomes, from insertion elements, from yeast chromosomal elements, from viruses such as baculoviruses, papova viruses, such as SV40, vaccinia viruses, adenoviruses, fowl pox viruses, pseudorabies viruses and retroviruses, and vectors derived from combinations thereof, such as those derived from plasmid and bacteriophage genetic elements, such as cosmids and phagemids. The expression systems may contain control regions that regulate as well as engender expression. Generally, any system or vector that is able to maintain, propagate or express a polynucleotide to produce a polypeptide in a host may be used. The appropriate polynucleotide sequence may be inserted into an expression system by any of a variety of well-known and routine techniques, such as, for example, those set forth in Sambrook et al., (ibid). Appropriate secretion signals may be incorporated into the desired polypeptide to allow secretion of the translated protein into the lumen of the endoplasmic reticulum, the periplasmic space or the extracellular environment. These signals may be endogenous to the polypeptide or they may be heterologous signals.

[0051] If a polypeptide of the present invention is to be expressed for use in screening assays, it is generally preferred that the polypeptide be produced at the surface of the cell. In this event, the cells may be harvested prior to use in the screening assay. If the polypeptide is secreted into the medium, the medium can be recovered in order to recover and purify the polypeptide. If produced intracellularly, the cells must first be lysed before the polypeptide is recovered.

[0052] Polypeptides of the present invention can be recovered and purified from recombinant cell cultures by well-known methods including ammonium sulfate or ethanol precipitation, acid extraction, anion or cation exchange chromatography, phosphocellulose chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography and lectin chromatography. Most preferably, high performance liquid chromatography is employed for purification. Well known techniques for refolding proteins may be employed to regenerate active conformation when the polypeptide is denatured during intracellular synthesis, isolation and/or purification.

[0053] Polynucleotides of the present invention may be used as diagnostic reagents, through detecting mutations in the associated gene. Detection of a mutated form of a gene is characterized by the polynucleotides set forth in the Sequence Listing in the cDNA or genomic sequence and which is associated with a dysfunction. Will provide a diagnostic tool that can add to, or define, a diagnosis of a disease, or susceptibility to a disease, which results from under-expression, over-expression or altered spatial or temporal expression of the gene. Individuals carrying mutations in the gene may be detected at the DNA level by a variety of techniques well known in the art.

[0054] Nucleic acids for diagnosis may be obtained from a subject's cells, such as from blood, urine, saliva, tissue biopsy or autopsy material. The genomic DNA may be used directly for detection or it may be amplified enzymatically by using PCR, preferably RT-PCR, or other amplification techniques prior to analysis. RNA or cDNA may also be used in similar fashion. Deletions and insertions can be detected by a change in size of the amplified product in comparison to the normal genotype. Point mutations can be identified by hybridizing amplified DNA to labeled nucleotide sequences of the genes set forth in Table I. Perfectly matched sequences can be distinguished from mismatched duplexes by RNase digestion or by differences in melting temperatures. DNA sequence difference may also be detected by alterations in the electrophoretic mobility of DNA fragments in gels, with or without denaturing agents, or by direct DNA sequencing (see, for instance, Myers et al., Science (1985) 230:1242). Sequence changes at specific locations may also be revealed by nuclease protection assays, such as RNase and S1 protection or the chemical cleavage method (see Cotton et al, Proc Natl Acad Sci USA (1985) 85:4397-4401).

[0055] An array of oligonucleotides probes comprising polynucleotide sequences or fragments thereof of the genes set forth in Table I can be constructed to conduct efficient screening of e.g., genetic mutations. Such arrays are preferably high density arrays or grids. Array technology methods are well known and have general applicability and can be used to address a variety of questions in molecular genetics including gene expression, genetic linkage, and genetic variability, see, for example, M. Chee et al., Science, 274, 610-613 (1996) and other references cited therein. Detection of abnormally decreased or increased levels of polypeptide or mRNA expression may also be used for diagnosing or determining susceptibility of a subject to a disease of the invention. Decreased or increased expression can be measured at the RNA level using any of the methods well known in the art for the quantitation of polynucleotides, such as, for example, nucleic acid amplification, for instance PCR, RT-PCR, RNase protection, Northern blotting and other hybridization methods. Assay techniques that can be used to determine levels of a protein, such as a polypeptide of the present invention, in a sample derived from a host are well-known to those of skill in the art. Such assay methods include radio-immunoassays, competitive-binding assays, Western Blot analysis and ELISA assays.

[0056] Thus in another aspect, the present invention relates to a diagnostic kit comprising:

[0057] (a) a polynucleotide of the present invention, preferably the nucleotide sequence set forth in the Sequence Listing, or a fragment or an RNA transcript thereof;

[0058] (b) a nucleotide sequence complementary to that of (a);

[0059] (c) a polypeptide of the present invention, preferably the polypeptide set forth in the Sequence Listing or a fragment thereof; or

[0060] (d) an antibody to a polypeptide of the present invention, preferably to the polypeptide set forth in the Sequence Listing.

[0061] It will be appreciated that in any such kit, (a), (b), (c) or (d) may comprise a substantial component. Such a kit will be of use in diagnosing a disease or susceptibility to a disease, particularly diseases of the invention, amongst others.

[0062] The polynucleotide sequences of the present invention are valuable for chromosome localisation studies. The sequences set forth in the Sequence Listing are specifically targeted to, and can hybridize with, a particular location on an individual human chromosome. The mapping of relevant sequences to chromosomes according to the present invention is an important first step in correlating those sequences with gene associated disease. Once a sequence has been mapped to a precise chromosomal location, the physical position of the sequence on the chromosome can be correlated with genetic map data. Such data are found in, for example, V. McKusick, Mendelian Inheritance in Man (available on-line through Johns Hopkins University Welch Medical Library). The relationship between genes and diseases that have been mapped to the same chromosomal region are then identified through linkage analysis (co-inheritance of physically adjacent genes). Precise human chromosomal localisations for a genomic sequence (gene fragment etc.) can be determined using Radiation Hybrid (RH) Mapping (Walter, M. Spillett, D., Thomas, P., Weissenbach, J., and Goodfellow, P., (1994) A method for constructing radiation hybrid maps of whole genomes, Nature Genetics 7, 22-28). A number of RH panels are available from Research Genetics (Huntsville, Ala., U.S.A.) e.g. the GeneBridge4 RH panel (Hum Mol Genet 1996 Mar; 5(3):339-46 A radiation hybrid map of the human genome. Gyapay G, Schmitt K, Fizames C, Jones H, Vega-Czarny N, Spillett D, Muselet D, Prud'Homme J F, Dib C, Auffray C, Morissette J, Weissenbach J, Goodfellow P N). To determine the chromosomal location of a gene using this panel, 93 PCRs are performed using primers designed from the gene of interest on RH DNAs. Each of these DNAs contains random human genomic fragments maintained in a hamster background (human/hamster hybrid cell lines). These PCRs result in 93 scores indicating the presence or absence of the PCR product of the gene of interest. These scores are compared with scores created using PCR products from genomic sequences of known location. This comparison is conducted at http://www.genome.wi.mit.edu/.

[0063] The polynucleotide sequences of the present invention are also valuable tools for tissue expression studies. Such studies allow the determination of expression patterns of polynucleotides of the present invention which may give an indication as to the expression patterns of the encoded polypeptides in tissues, by detecting the mRNAs that encode them. The techniques used are well known in the art and include in situ hybridization techniques to clones arrayed on a grid, such as cDNA microarray hybridization (Schena et al, Science, 270, 467-470, 1995 and Shalon et al, Genome Res, 6, 639-645, 1996) and nucleotide amplification techniques such as PCR. A preferred method uses the TAQMAN (Trade mark) technology available from Perkin Elmer. Results from these studies can provide an indication of the normal function of the polypeptide in the organism. In addition, comparative studies of the normal expression pattern of mRNAs with that of mRNAs encoded by an alternative form of the same gene (for example, one having an alteration in polypeptide coding potential or a regulatory mutation) can provide valuable insights into the role of the polypeptides of the present invention, or that of inappropriate expression thereof in disease. Such inappropriate expression may be of a temporal, spatial or simply quantitative nature.

[0064] A further aspect of the present invention relates to antibodies. The polypeptides of the invention or their fragments, or cells expressing them, can be used as immunogens to produce antibodies that are immunospecific for polypeptides of the present invention. The term “immunospecific” means that the antibodies have substantially greater affinity for the polypeptides of the invention than their affinity for other related polypeptides in the prior art.

[0065] Antibodies generated against polypeptides of the present invention may be obtained by administering the polypeptides or epitope-bearing fragments, or cells to an animal, preferably a non-human animal, using routine protocols. For preparation of monoclonal antibodies, any technique which provides antibodies produced by continuous cell line cultures can be used. Examples include the hybridoma technique (Kohler, G. and Milstein, C., Nature (1975) 256:495-497), the trioma technique, the human B-cell hybridoma technique (Kozbor et al, Immunology Today (1983) 4:72) and the EBV-hybridoma technique (Cole et Al, Monoclonal Antibodies and Cancer Therapy, 77-96, Alan R. Liss, Inc., 1985).

[0066] Techniques for the production of single chain antibodies, such as those described in U.S. Pat. No. 4,946,778, can also be adapted to produce single chain antibodies to polypeptides of this invention. Also, transgenic mice, or other organisms, including other mammals, may be used to express humanized antibodies.

[0067] The above-described antibodies may be employed to isolate or to identify clones expressing the polypeptide or to purify the polypeptides by affinity chromatography. Antibodies against polypeptides of the present invention may also be employed to treat diseases of the invention, amongst others.

[0068] Polypeptides and polynucleotides of the present invention may also be used as vaccines. Accordingly, in a further aspect, the present invention relates to a method for inducing an immunological response in a mammal that comprises inoculating the mammal with a polypeptide of the present invention, adequate to produce antibody and/or T cell immune response, including, for example, cytokine-producing T cells or cytotoxic T cells, to protect said animal from disease, whether that disease is already established within the individual or not. An immunological response in a mammal may also be induced by a method comprises delivering a polypeptide of the present invention via a vector directing expression of the polynucleotide and coding for the polypeptide in vivo in order to induce such an immunological response to produce antibody to protect said animal from diseases of the invention. One way of administering the vector is by accelerating it into the desired cells as a coating on particles or otherwise. Such nucleic acid vector may comprise DNA, RNA, a modified nucleic acid, or a DNA/RNA hybrid. For use a vaccine, a polypeptide or a nucleic acid vector will be normally provided as a vaccine formulation (composition). The formulation may further comprise a suitable carrier. Since a polypeptide may be broken down in the stomach, it is preferably administered parenterally (for instance, subcutaneous, intramuscular, intravenous, or intra-dermal injection). Formulations suitable for parenteral administration include aqueous and non-aqueous sterile injection solutions that may contain anti-oxidants, buffers, bacteriostats and solutes that render the formulation instonic with the blood of the recipient; and aqueous and non-aqueous sterile suspensions that may include suspending agents or thickening agents. The formulations may be presented in unit-dose or multi-dose containers, for example, sealed ampoules and vials and may be stored in a freeze-dried condition requiring only the addition of the sterile liquid carrier immediately prior to use. The vaccine formulation may also include adjuvant systems for enhancing the immunogenicity of the formulation, such as oil-in water systems and other systems known in the art. The dosage will depend on the specific activity of the vaccine and can be readily determined by routine experimentation.

[0069] Polypeptides of the present invention have one or more biological functions that are of relevance in one or more disease states, in particular the diseases of the invention hereinbefore mentioned. It is therefore useful to identify compounds that stimulate or inhibit the function or level of the polypeptide. Accordingly, in a further aspect, the present invention provides for a method of screening compounds to identify those that stimulate or inhibit the function or level of the polypeptide. Such methods identify agonists or antagonists that may be employed for therapeutic and prophylactic purposes for such diseases of the invention as hereinbefore mentioned. Compounds may be identified from a variety of sources, for example, cells, cell-free preparations, chemical libraries, collections of chemical compounds, and natural product mixtures. Such agonists or antagonists so-identified may be natural or modified substrates, ligands, receptors, enzymes, etc., as the case may be, of the polypeptide; a structural or functional mimetic thereof (see Coligan et al, Current Protocols in Immunology 1(2): Chapter 5 (1991)) or a small molecule. Such small molecules preferably have a molecular weight below 2,000 daltons, more preferably between 300 and 1,000 daltons, and most preferably between 400 and 700 daltons. It is preferred that these small molecules are organic molecules.

[0070] The screening method may simply measure the binding of a candidate compound to the polypeptide, or to cells or membranes bearing the polypeptide, or a fusion protein thereof, by means of a label directly or indirectly associated with the candidate compound. Alternatively, the screening method may involve measuring or detecting (qualitatively or quantitatively) the competitive binding of a candidate compound to the polypeptide against a labeled competitor (e.g. agonist or antagonist). Further, these screening methods may test whether the candidate compound results in a signal generated by activation or inhibition of the polypeptide, using detection systems appropriate to the cells bearing the polypeptide. Inhibitors of activation are generally assayed in the presence of a known agonist and the effect on activation by the agonist by the presence of the candidate compound is observed. Further, the screening methods may simply comprise the steps of mixing a candidate compound with a solution containing a polypeptide of the present invention, to form a mixture, measuring an activity of the genes set forth in Table I in the mixture, and comparing activity of the mixture of the genes set forth in Table I to a control mixture which contains no candidate compound.

[0071] Polypeptides of the present invention may be employed in conventional low capacity screening methods and also in high-throughput screening (HTS) formats. Such HTS formats include not only the well-established use of 96- and, more recently, 384-well microtiter plates but also emerging methods such as the nanowell method described by Schullek et al, Anal Biochem., 246, 20-29, (1997). Fusion proteins, such as those made from Fc portion and polypeptide of the genes set forth in Table I, as hereinbefore described, can also be used for high-throughput screening assays to identify antagonists for the polypeptide of the present invention (see D. Bennett et al., J Mol Recognition, 8:52-58 (1995); and K. Johanson et al., J Biol Chem, 270(16):9459-9471 (1995)).

[0072] The polynucleotides, polypeptides and antibodies to the polypeptide of the present invention may also be used to configure screening methods for detecting the effect of added compounds on the production of mRNA and polypeptide in cells. For example, an ELISA assay may be constructed for measuring secreted or cell associated levels of polypeptide using monoclonal and polyclonal antibodies by standard methods known in the art. This can be used to discover agents that may inhibit or enhance the production of polypeptide (also called antagonist or agonist, respectively) from suitably manipulated cells or tissues.

[0073] A polypeptide of the present invention may be used to identify membrane bound or soluble receptors, if any, through standard receptor binding techniques known in the art. These include, but are not limited to, ligand binding and crosslinking assays in which the polypeptide is labeled with a radioactive isotope (for instance, ¹²⁵I), chemically modified (for instance, biotinylated), or fused to a peptide sequence suitable for detection or purification, and incubated with a source of the putative receptor (cells, cell membranes, cell supernatants, tissue extracts, bodily fluids). Other methods include biophysical techniques such as surface plasmon resonance and spectroscopy. These screening methods may also be used to identify agonists and antagonists of the polypeptide that compete with the binding of the polypeptide to its receptors, if any. Standard methods for conducting such assays are well understood in the art.

[0074] Examples of antagonists of polypeptides of the present invention include antibodies or, in some cases, oligonucleotides or proteins that are closely related to the ligands, substrates, receptors, enzymes, etc., as the case may be, of the polypeptide, e.g., a fragment of the ligands, substrates, receptors, enzymes, etc.; or a small molecule that bind to the polypeptide of the present invention but do not elicit a response, so that the activity of the polypeptide is prevented.

[0075] Screening methods may also involve the use of transgenic technology and the genes set forth in Table I. The art of constructing transgenic animals is well established. For example, the genes set forth in Table I may be introduced through microinjection into the male pronucleus of fertilized oocytes, retroviral transfer into pre- or post-implantation embryos, or injection of genetically modified, such as by electroporation, embryonic stem cells into host blastocysts. Particularly useful transgenic animals are so-called “knock-in” animals in which an animal gene is replaced by the human equivalent within the genome of that animal. Knock-in transgenic animals are useful in the drug discovery process, for target validation, where the compound is specific for the human target. Other useful transgenic animals are so-called “knock-out” animals in which the expression of the animal ortholog of a polypeptide of the present invention and encoded by an endogenous DNA sequence in a cell is partially or completely annulled. The gene knock-out may be targeted to specific cells or tissues, may occur only in certain cells or tissues as a consequence of the limitations of the technology, or may occur in all, or substantially all, cells in the animal. Transgenic animal technology also offers a whole animal expression-cloning system in which introduced genes are expressed to give large amounts of polypeptides of the present invention

[0076] Screening kits for use in the above described methods form a further aspect of the present invention. Such screening kits comprise:

[0077] (a) a polypeptide of the present invention;

[0078] (b) a recombinant cell expressing a polypeptide of the present invention;

[0079] (c) a cell membrane expressing a polypeptide of the present invention; or

[0080] (d) an antibody to a polypeptide of the present invention; which polypeptide is preferably that set forth in the Sequence Listing.

[0081] It will be appreciated that in any such kit, (a), (b), (c) or (d) may comprise a substantial component.

Glossary

[0082] The following definitions are provided to facilitate understanding of certain terms used frequently hereinbefore.

[0083] “Antibodies” as used herein includes polyclonal and monoclonal antibodies, chimeric, single chain, and humanized antibodies, as well as Fab fragments, including the products of an Fab or other immunoglobulin expression library.

[0084] “Isolated” means altered “by the hand of man” from its natural state, i.e., if it occurs in nature, it has been changed or removed from its original environment, or both. For example, a polynucleotide or a polypeptide naturally present in a living organism is not “isolated,” but the same polynucleotide or polypeptide separated from the coexisting materials of its natural state is “isolated”, as the term is employed herein. Moreover, a polynucleotide or polypeptide that is introduced into an organism by transformation, genetic manipulation or by any other recombinant method is “isolated” even if it is still present in said organism, which organism may be living or non-living.

[0085] “Secreted protein activity or secreted polypeptide activity” or “biological activity of the secreted protein or secreted polypeptide” refers to the metabolic or physiologic function of said secreted protein including similar activities or improved activities or these activities with decreased undesirable side-effects. Also included are antigenic and immunogenic activities of said secreted protein.

[0086] “Secreted protein gene” refers to a polynucleotide comprising any of the attached nucleotide sequences or allelic variants thereof and/or their complements.

[0087] “Polynucleotide” generally refers to any polyribonucleotide (RNA) or polydeoxribonucleotide (DNA), which may be unmodified or modified RNA or DNA. “Polynucleotides” include, without limitation, single- and double-stranded DNA, DNA that is a mixture of single- and double-stranded regions, single- and double-stranded RNA, and RNA that is mixture of single- and double-stranded regions, hybrid molecules comprising DNA and RNA that may be single-stranded or, more typically, double-stranded or a mixture of single- and double-stranded regions. In addition, “polynucleotide” refers to triple-stranded regions comprising RNA or DNA or both RNA and DNA. The term “polynucleotide” also includes DNAs or RNAs containing one or more modified bases and DNAs or RNAs with backbones modified for stability or for other reasons. “Modified” bases include, for example, tritylated bases and unusual bases such as inosine. A variety of modifications may be made to DNA and RNA; thus, “polynucleotide” embraces chemically, enzymatically or metabolically modified forms of polynucleotides as typically found in nature, as well as the chemical forms of DNA and RNA characteristic of viruses and cells. “Polynucleotide” also embraces relatively short polynucleotides, often referred to as oligonucleotides.

[0088] “Polypeptide” refers to any polypeptide comprising two or more amino acids joined to each other by peptide bonds or modified peptide bonds, i.e., peptide isosteres. “Polypeptide” refers to both short chains, commonly referred to as peptides, oligopeptides or oligomers, and to longer chains, generally referred to as proteins. Polypeptides may contain amino acids other than the 20 gene-encoded amino acids. “Polypeptides” include amino acid sequences modified either by natural processes, such as post-translational processing, or by chemical modification techniques that are well known in the art. Such modifications are well described in basic texts and in more detailed monographs, as well as in a voluminous research literature. Modifications may occur anywhere in a polypeptide, including the peptide backbone, the amino acid side-chains and the amino or carboxyl termini. It will be appreciated that the same type of modification may be present to the same or varying degrees at several sites in a given polypeptide. Also, a given polypeptide may contain many types of modifications. Polypeptides may be branched as a result of ubiquitination, and they may be cyclic, with or without branching. Cyclic, branched and branched cyclic polypeptides may result from post-translation natural processes or may be made by synthetic methods. Modifications include acetylation, acylation, ADP-ribosylation, amidation, biotinylation, covalent attachment of flavin, covalent attachment of a heme moiety, covalent attachment of a nucleotide or nucleotide derivative, covalent attachment of a lipid or lipid derivative, covalent attachment of phosphotidylinositol, cross-linking, cyclization, disulfide bond formation, demethylation, formation of covalent cross-links, formation of cystine, formation of pyroglutamate, formylation, gamma-carboxylation, glycosylation, GPI anchor formation, hydroxylation, iodination, methylation, myristoylation, oxidation, proteolytic processing, phosphorylation, prenylation, racemization, selenoylation, sulfation, transfer-RNA mediated addition of amino acids to proteins such as arginylation, and ubiquitination (see, for instance, Proteins—Structure and Molecular Properties, 2nd Ed., T. E. Creighton, W. H. Freeman and Company, New York, 1993; Wold, F., Post-translational Protein Modifications: Perspectives and Prospects, 1-12, in Post-translational Covalent Modification of Proteins, B. C. Johnson, Ed., Academic Press, New York, 1983; Seifter et al., “Analysis for protein modifications and nonprotein cofactors”, Meth Enzymol, 182, 626-646, 1990, and Rattan et Al, “Protein Synthesis: Post-translational Modifications and Aging”, Ann NY Acad Sci, 663, 48-62, 1992).

[0089] “Fragment” of a polypeptide sequence refers to a polypeptide sequence that is shorter than the reference sequence but that retains essentially the same biological function or activity as the reference polypeptide. “Fragment” of a polynucleotide sequence refers to a polynucleotide sequence that is shorter than the reference sequence set forth in the Sequence Listing.

[0090] “Variant” refers to a polynucleotide or polypeptide that differs from a reference polynucleotide or polypeptide, but retains the essential properties thereof. A typical variant of a polynucleotide differs in nucleotide sequence from the reference polynucleotide. Changes in the nucleotide sequence of the variant may or may not alter the amino acid sequence of a polypeptide encoded by the reference polynucleotide. Nucleotide changes may result in amino acid substitutions, additions, deletions, fusions and truncations in the polypeptide encoded by the reference sequence, as discussed below. A typical variant of a polypeptide differs in amino acid sequence from the reference polypeptide. Generally, alterations are limited so that the sequences of the reference polypeptide and the variant are closely similar overall and, in many regions, identical. A variant and reference polypeptide may differ in amino acid sequence by one or more substitutions, insertions, deletions in any combination. A substituted or inserted amino acid residue may or may not be one encoded by the genetic code. Typical conservative substitutions include Gly, Ala; Val, Ile, Leu; Asp, Glu; Asn, Gln; Ser, Thr; Lys, Arg; and Phe and Tyr. A variant of a polynucleotide or polypeptide may be naturally occurring such as an allele, or it may be a variant that is not known to occur naturally. Non-naturally occurring variants of polynucleotides and polypeptides may be made by mutagenesis techniques or by direct synthesis. Also included as variants are polypeptides having one or more post-translational modifications, for instance glycosylation, phosphorylation, methylation, ADP ribosylation and the like. Embodiments include methylation of the N-terminal amino acid, phosphorylations of serines and threonines and modification of C-terminal glycines.

[0091] “Allele” refers to one of two or more alternative forms of a gene occurring at a given locus in the genome.

[0092] “Polymorphism” refers to a variation in nucleotide sequence (and encoded polypeptide sequence, if relevant) at a given position in the genome within a population.

[0093] “Single Nucleotide Polymorphism” (SNP) refers to the occurrence of nucleotide variability at a single nucleotide position in the genome, within a population. An SNP may occur within a gene or within intergenic regions of the genome. SNPs can be assayed using Allele Specific Amplification (ASA). For the process at least 3 primers are required. A common primer is used in reverse complement to the polymorphism being assayed. This common primer can be between 50 and 1500 bps from the polymorphic base. The other two (or more) primers are identical to each other except that the final 3′ base wobbles to match one of the two (or more) alleles that make up the polymorphism. Two (or more) PCR reactions are then conducted on sample DNA, each using the common primer and one of the Allele Specific Primers.

[0094] “Splice Variant” as used herein refers to cDNA molecules produced from RNA molecules initially transcribed from the same genomic DNA sequence but which have undergone alternative RNA splicing. Alternative RNA splicing occurs when a primary RNA transcript undergoes splicing, generally for the removal of introns, which results in the production of more than one mRNA molecule each of that may encode different amino acid sequences. The term splice variant also refers to the proteins encoded by the above cDNA molecules.

[0095] “Identity” reflects a relationship between two or more polypeptide sequences or two or more polynucleotide sequences, determined by comparing the sequences. In general, identity refers to an exact nucleotide to nucleotide or amino acid to amino acid correspondence of the two polynucleotide or two polypeptide sequences, respectively, over the length of the sequences being compared.

[0096] “% Identity”—For sequences where there is not an exact correspondence, a “% identity” may be determined. In general, the two sequences to be compared are aligned to give a maximum correlation between the sequences. This may include inserting “gaps” in either one or both sequences, to enhance the degree of alignment. A % identity may be determined over the whole length of each of the sequences being compared (so-called global alignment), that is particularly suitable for sequences of the same or very similar length, or over shorter, defined lengths (so-called local alignment), that is more suitable for sequences of unequal length.

[0097] “Similarity” is a further, more sophisticated measure of the relationship between two polypeptide sequences. In general, “similarity” means a comparison between the amino acids of two polypeptide chains, on a residue by residue basis, taking into account not only exact correspondences between a between pairs of residues, one from each of the sequences being compared (as for identity) but also, where there is not an exact correspondence, whether, on an evolutionary basis, one residue is a likely substitute for the other. This likelihood has an associated “score” from which the “% similarity” of the two sequences can then be determined.

[0098] Methods for comparing the identity and similarity of two or more sequences are well known in the art. Thus for instance, programs available in the Wisconsin Sequence Analysis Package, version 9.1 (Devereux J et al, Nucleic Acids Res, 12, 387-395, 1984, available from Genetics Computer Group, Madison, Wis., U.S.A.), for example the programs BESTFIT and GAP, may be used to determine the % identity between two polynucleotides and the % identity and the % similarity between two polypeptide sequences. BESTFIT uses the “local homology” algorithm of Smith and Waterman (J Mol Biol, 147,195-197, 1981, Advances in Applied Mathematics, 2, 482-489, 1981) and finds the best single region of similarity between two sequences. BESTFIT is more suited to comparing two polynucleotide or two polypeptide sequences that are dissimilar in length, the program assuming that the shorter sequence represents a portion of the longer. In comparison, GAP aligns two sequences, finding a “maximum similarity”, according to the algorithm of Neddleman and Wunsch (J Mol Biol, 48,443-453, 1970). GAP is more suited to comparing sequences that are approximately the same length and an alignment is expected over the entire length. Preferably, the parameters “Gap Weight” and “Length Weight” used in each program are 50 and 3, for polynucleotide sequences and 12 and 4 for polypeptide sequences, respectively. Preferably, % identities and similarities are determined when the two sequences being compared are optimally aligned.

[0099] Other programs for determining identity and/or similarity between sequences are also known in the art, for instance the BLAST family of programs (Altschul S F et al, J Mol Biol, 215, 403-410, 1990, Altschul S F et al, Nucleic Acids Res., 25:389-3402, 1997, available from the National Center for Biotechnology Information (NCBI), Bethesda, Md., U.S.A. and accessible through the home page of the NCBI at www.ncbi.nlm.nih.gov) and FASTA (Pearson W R, Methods in Enzymology, 183, 63-99, 1990; Pearson W R and Lipman D J, Proc Nat Acad Sci USA, 85, 2444-2448,1988, available as part of the Wisconsin Sequence Analysis Package).

[0100] Preferably, the BLOSUM62 amino acid substitution matrix (Henikoff S and Henikoff J G, Proc. Nat. Acad Sci. USA, 89, 10915-10919, 1992) is used in polypeptide sequence comparisons including where nucleotide sequences are first translated into amino acid sequences before comparison.

[0101] Preferably, the program BESTFIT is used to determine the % identity of a query polynucleotide or a polypeptide sequence with respect to a reference polynucleotide or a polypeptide sequence, the query and the reference sequence being optimally aligned and the parameters of the program set at the default value, as hereinbefore described.

[0102] “Identity Index” is a measure of sequence relatedness which may be used to compare a candidate sequence (polynucleotide or polypeptide) and a reference sequence. Thus, for instance, a candidate polynucleotide sequence having, for example, an Identity Index of 0.95 compared to a reference polynucleotide sequence is identical to the reference sequence except that the candidate polynucleotide sequence may include on average up to five differences per each 100 nucleotides of the reference sequence. Such differences are selected from the group consisting of at least one nucleotide deletion, substitution, including transition and transversion, or insertion. These differences may occur at the 5′ or 3′ terminal positions of the reference polynucleotide sequence or anywhere between these terminal positions, interspersed either individually among the nucleotides in the reference sequence or in one or more contiguous groups within the reference sequence. In other words, to obtain a polynucleotide sequence having an Identity Index of 0.95 compared to a reference polynucleotide sequence, an average of up to 5 in every 100 of the nucleotides of the in the reference sequence may be deleted, substituted or inserted, or any combination thereof, as hereinbefore described. The same applies mutatis mutandis for other values of the Identity Index, for instance 0.96, 0.97, 0.98 and 0.99.

[0103] Similarly, for a polypeptide, a candidate polypeptide sequence having, for example, an Identity Index of 0.95 compared to a reference polypeptide sequence is identical to the reference sequence except that the polypeptide sequence may include an average of up to five differences per each 100 amino acids of the reference sequence. Such differences are selected from the group consisting of at least one amino acid deletion, substitution, including conservative and non-conservative substitution, or insertion. These differences may occur at the amino- or carboxy-terminal positions of the reference polypeptide sequence or anywhere between these terminal positions, interspersed either individually among the amino acids in the reference sequence or in one or more contiguous groups within the reference sequence. In other words, to obtain a polypeptide sequence having an Identity Index of 0.95 compared to a reference polypeptide sequence, an average of up to 5 in every 100 of the amino acids in the reference sequence may be deleted, substituted or inserted, or any combination thereof, as hereinbefore described. The same applies mutatis mutandis for other values of the Identity Index, for instance 0.96, 0.97, 0.98 and 0.99.

[0104] The relationship between the number of nucleotide or amino acid differences and the Identity Index may be expressed in the following equation:

n _(a) ≦x _(a)−(x _(a) ·I)

[0105] in which:

[0106] n_(a) is the number of nucleotide or amino acid differences,

[0107] x_(a) is the total number of nucleotides or amino acids in a sequence set forth in the Sequence Listing,

[0108] I is the Identity Index,

[0109] · is the symbol for the multiplication operator, and in which any non-integer product of x_(a) and I is rounded down to the nearest integer prior to subtracting it from x_(a).

[0110] “Homolog” is a generic term used in the art to indicate a polynucleotide or polypeptide sequence possessing a high degree of sequence relatedness to a reference sequence. Such relatedness may be quantified by determining the degree of identity and/or similarity between the two sequences as hereinbefore defined. Falling within this generic term are the terms “ortholog”, and “paralog”. “Ortholog” refers to a polynucleotide or polypeptide that is the functional equivalent of the polynucleotide or polypeptide in another species. “Paralog” refers to a polynucleotide or polypeptide that within the same species which is functionally similar.

[0111] “Fusion protein” refers to a protein encoded by two, often unrelated, fused genes or fragments thereof. In one example, EP-A-0 464 533-A discloses fusion proteins comprising various portions of constant region of immunoglobulin molecules together with another human protein or part thereof. In many cases, employing an immunoglobulin Fc region as a part of a fusion protein is advantageous for use in therapy and diagnosis resulting in, for example, improved pharmacokinetic properties [see, e.g., EP-A 0232 262]. On the other hand, for some uses it would be desirable to be able to delete the Fc part after the fusion protein has been expressed, detected and purified.

[0112] All publications and references, including but not limited to patents and patent applications, cited in this specification are herein incorporated by reference in their entirety as if each individual publication or reference were specifically and individually indicated to be incorporated by reference herein as being fully set forth. Any patent application to which this application claims priority is also incorporated by reference herein in its entirety in the manner described above for publications and references. TABLE I GSK Corresponding Gene Nucleic Acid Protein Gene Name ID SEQ ID NO's SEQ ID NO's sbgTango79a 14898 SEQ ID NO:1 SEQ ID NO:24 sbgPRO331a 14908 SEQ ID NO:2 SEQ ID NO:25 sbghPYYa 24835 SEQ ID NO:3 SEQ ID NO:26 sbghGTa 25306 SEQ ID NO:4 SEQ ID NO:27 SB-HDGF 42748 SEQ ID NO:5 SEQ ID NO:28 SEQ ID NO:6 SEQ ID NO:29 SBhACRP30a 34718 SEQ ID NO:7 SEQ ID NO:30 SEQ ID NO:8 SEQ ID NO:31 sbg35069DBIa 35069 SEQ ID NO:9 SEQ ID NO:32 sbg14862SPERCTa 14862 SEQ ID NO:10 SEQ ID NO:33 SEQ ID NO:11 SEQ ID NO:34 sbg24878SIa 24878 SEQ ID NO:12 SEQ ID NO:35 SEQ ID NO:13 SEQ ID NO:36 sbg34976IGBa 34976 SEQ ID NO:14 SEQ ID NO:37 sbg41608HDGFa 41608 SEQ ID NO:15 SEQ ID NO:38 sbg66804SPARCra 66804 SEQ ID NO:16 SEQ ID NO:39 SEQ ID NO:17 SEQ ID NO:40 sbg72825FOLATEa 72825 SEQ ID NO:18 SEQ ID NO:41 SBhPRO221 73255 SEQ ID NO:19 SEQ ID NO:42 sbg77153CYSa 77153 SEQ ID NO:20 SEQ ID NO:43 SBh80014.IAPa 80014 SEQ ID NO:21 SEQ ID NO:44 SEQ ID NO:22 SEQ ID NO:45 sbgFGF-19b 68602 SEQ ID NO:23 SEQ ID NO:46

[0113] TABLE II Closet Closet Cell Polynuclotide by Polypeptide by Localization Gene Name Gene Family homology homology (by homology) sbgTango79a Slit-like GB: AC004152 The human Tango-79 membrane- membrane Joint Genome Institute, protein, bound glycoprotein Lawrence Livermore geneseqp: W84596 National Laboratory, Patent number and 7000 East Ave., publication date: Livermore, CA 94551, WO9906427-A1 Feb. 11, 1999 USA sbgPRO331a Slit-like GB: AC008039 The human protein membrane- membrane Human Genome Center, PRO331, bound glycoprotein University of geneseqp: Y13394 Washington, Box Patent number and 352145, Seattle, WA publication date: 98195, USA WO9914328-A2 Mar. 25, 1999 sbghPYYa Peptide YY GB: AJ239323 Human peptideYY, secreted Max-Planck-Institute for gi: 1172796 Molecular Genetics Kohri, K., Nata, K., Yonekura, H., Nagai, A., Konno, K. and Okamoto, H. Biochim. Biophys. Acta 1173 (3), 345-349 (1993) sbghGTa Gonadotropin GB: AL049871 Pacific herring secreted beta chain Genoscope - Centre gonadotropin II- National de beta, gi: 4200297 Sequencage: BP Power, M. E, 19191006 EVRY cedex Carolsfield, J, Wallis, G. P. FRANCE and Sherwood, N. M. J. Fish Biol. 50, 315-323 (1997) SB-HDGF Hepatoma JGI: CIT978SKB_50L17 Mouse HDGF, gi: secreted derived growth Found at Joint Genome 2558501 factor (HDGF) Institute Biochem. Biophys. Res. Commun. 238(1), 26-32, 1997 SBhACRP30a Complement GB: AC007016 Mouse30 Kda adipocyte secreted C1q/TNF Submitted (May 8, 1999) complement-related by Department of protein ACRP30, gi: Genetics, Stanford 1051268 Human Genome Center, P. Sherer et al., J. Biol. 855 Miranda Avenue, Chem. 270(18), 10697- Palo, CA 94304 10703, 1996. sbg35069DBIa Neuropeptide EMBL: AC010999 ACYL-COA- cytosolic Submitted (Sep. 29, 1999) BINDING PROTEIN by Multimegabase HOMOLOG (ACBP), Sequencing Center, gi: 1168274 University of Lihrmann, I. et al. Proc. Natl. Washington, P.O. Box Acad. Sci. U.S.A. 91(15), 357730. Seattle, WA 6899-6903 (1994) 98195 sbg14862SPERCTa speract GB: AC005522 gp-340, a putative membrane- receptor (WU: H_DJ1129E2) opsonin receptor for lung bound submitted by Genome surfactant, gi: 5733598 Sequencing Center, Holmskov U, Washington University, Mollenhauer J, Madsen J, School of Medicine, Vitved L, Gronlund J, 4444 Forest Park Tornoe I, Kliem A, Reid Parkway, K B, Poustka A, Skjodt K, St. Lous, MO 63108, Proc Natl Acad Sci USA USA Sep. 14, 1999; 96(19): 10794-9. sbg24878SIa laminin type SC: AL109804 Mouse sialoadhesin gene, secreted EGF, EGF2, found at Sanger Center gi: 2769747 ldlra2, dlra2, Mucklow S, Gordon S, ldlra1 and Crocker P R. Mamm EGF1 Genome December 1997; 8(12): 934-7 sbg34976IGBa Slit-like GB: AC010931 Immunoglobulin membrane- membrane Submitted (Jan. 30, superfamily containing bound glycoprotein 1999) by Genome leucine-rich repeat, Sequencing Center, gi: 5031809 Washington University Nagasawa A, Kubota R, School of Medicine, Imamura Y, Nagamine K, 4444 Forest Park Wang Y, Asakawa S, Parkway, St. Louis, MO Kudoh J, 63108, USA Minoshima S, Mashima Y, Oguchi Y, Shimizu N, Genomics Sep. 15, 1997; 44(3): 273-9 sbg41608HDGFa Hepatoma- GB: AL033539 Bovine hepatoma-derived secreted derived growth Submitted by Sanger growth factor, gi: 945419 factor Center Biochem. Biophys. Res. Hinxton, Commun. 238(1): 26-32, Cambridgeshire, CB10 1997 1SA, UK sbg66804SPARCra Sparc-related GB: AL135747 Mouse SPARC-related membrane- protein Submitted by Genoscope - rpotein, gi: 5305327 bound Centre National de Submitted (Jun. 5, 1998) Sequencage: BP by GeneCraft, Treskowst. 19191006 EVRY cedex, 10, Muenster 48163, FRANCE Germany. sbg72825FOLATEa Folate receptor SB: AP000765 Sus scrofa membrance- membrane- Submitted (NOV. 25. bound folate binding bound 1999) by Masahira protein, gi: 4928859 Hattori, The Institute of Vallet, J. L., Smith, T. P. L., Physical and Sontegard, T., ChemicalResearch Pearson, P. L., Christenson, (RIKEN), Genomic R. K. and Sciences Center (GSC); Klemcke, H. G. Biol. 1-7-22 Suehiro-chou, Reprod. 61(2): 372 (1999) Tsurumi-ku, Yokohama, Kanagawa 230-0045, Japan SBhPRO221 Slit-like GB: AP001065 New isolated human gene, membrane- membrane Submitted (JAN. 12, geneseqp: Y13356. bound glycoprotein 2000) by Nobuyoshi WO9914328-A2, Chen, J. Shimizu, Keio Goddard, A., Yuan, J., University, School of Genentech Inc. Jun. 25, Medicine, Molecular 1999 GPS Biology; 35 Shinanomachi, Shinjuku- ku, Tokyo 160-8582, Japan sbg77153CYSa Testatin GB: AL121894 Mouse testatin precursor, secreted Submitted by Sanger gi: 3928491 Center Tohonen, V., Osterlund, C. and Nordqvist, K. Proc. Natl. Acad. Sci. U.S.A. 95 (24), 14208-14213 (1998). SBh80014.IAPa Inhibitor of GB: AL121827 human putative inhibitor cytosolic apoptosis Submitted by Sanger of apoptosis, gi: 3914339 protein (IAP) Center C. Stehlik et al, Biochem. Biophys. Res. Commun. 243(3), 827-832, 1998 sbgFGF-19b Fibroblast GB: AB018122Homo FGF-19 (gi secreted Growth Factor sapiens mRNA for FGF- 5668601, gi 4826726, 19, complete cds gi 4514718, (Nishimura, T., (Nishimura, T., Utsunomiya,Y ., Utsunomiya, Y., Hoshikawa, M., Hoshikawa, M., Ohuchi, H. Ohuchi, H. and Itoh, N. and Itoh, N. Structure and Structure and expression expression of a novel of a novel human FGF, human FGF, FGF-19, FGF-19, expressed in the expressed in the fetal fetal brain. Biochim. brain. Biochim. Biophys. Biophys. Acta 1444 (1), Acta 1444 (1), 148-151 148-151 (1999)) (1999))

[0114] TABLE III Gene Name Uses Associated Diseases sbgTango79a An embodiment of the invention is the use of Alzheimers disease, ALS, abnormal sbgTango79a, a secreted protein, in the diagnosis and keratinocyte differentiation, anti treatment of Tango-associated diseases and thrombosis, atrophia areata, cell involvement in gastrointestinal ulceration. growth, congenital microvillus Close Homologs of sbgTango79a are Tango 79 and atrophy, dermal scarring, PRO227. enterocolitis, cancer, gastrointestinal ulceration, neuropathy, Parkinson's disease, psoriasis, skin diseases, Usher's syndrome, wound healing, and Zollinger-Ellison syndrome sbgPRO331a An embodiment of the invention is the use of Alzheimers disease, ALS, abnormal sbgPRO331a, in the treatment of gastrointestinal keratinocyte differentiation, anti- ulceration and involved in nutritional activity, thrombosis, atrophia areata, cell cytokine and cell proliferation/differentiation growth, hematopoietic disease, activity, immune stimulating (e.g. as vaccines) or diseases of the immune system, suppressing activity, haematopoiesis regulating inflammation, congenital activity, tissue growth activity, activin/inhibin microvillus atrophy, dermal activity, chemotactic/chemokinetic activity, scarring, enterocolitis, cancer, haemostatic and thrombolytic activity, gastrointestinal ulceration, receptor/ligand activity, anti-inflammatory activity, neuropathy, Parkinson's disease, cadherin/tumour invasion suppressor activity, and psoriasis, skin diseases, Usher's tumour inhibition activity. The polynucleotides of syndrome, wound healing, and sbgPRO331a may also be useful for gene therapy. Zollinger-Ellison syndrome Close Homologs of sbgPRO331a are PRO331 and AS209_1. sbghPYYa An embodiment of the invention is the use of Anxiety, schizophrenia, feeding sbghPYYa, to identify new receptors and receptor disorders, anorexia, depression, agonists, antagonists, or protein agents. A close grooming, stretching, yawning, homolog of sbghPYYa is Peptide YY precursor, a social, sexual and rewarded clinically significant member of the neuropeptide behavior, chronic and acute family which include peptides such as pancreatic inflammation, cardiovasuclar hormone, neuropeptide Y (NPY) and peptide YY disease, sleep disorder, learning and (PYY). These neuropeptides are ligands for G- memory alteration and altered protein coupled receptors. immune response, cancer, seizure, stroke, migraine, asthma, neuropathy and aging sbghGTa Human gonadotropin most similar to luteinizing Sexual disorders, infertility, hormone, sbghGTa, is exploitable in similar ways to blocking fertility, hypogonadism, luteinizing hormone or its releasing hormone. prostate and other cancers, treatment Luteinizing hormone is helpful in ovulation of transsexuals induction for reproductive procedures (Fertil. Steril. 1999. 71(3): 405-414). Luteinizing hormone- releasing hormone and its agonists are exploited to reduce androgen levels in prostate cancer (Oncology, 1998. 12(4): 499-505). Gonadotropin releasing hormone use is helpful in polycystic ovary syndrome (Eur. J. Contracept. Reprod. Health Care. 1997. 2(4): 213-224). SB-HDGF An embodiment of the invention is the use of SB- Cancer, inflammation, defective HDGF, to control cell growth and regulation of cell immune response, cardiovadcular differentiation. Hepatoma-derived growth factors are disease, growth abnormalities members of a diverse family of cytokines. Like other cytokines, they are peptides involved in the control of cell growth regulation, differentiation and function (Thomsan, The Cytokine Handbook, 2nd edition, Academic Press, Harcourt Brace & co. publishers, London). Another embodiment of the invention is the use of SB-HDGF for diagnosis or therapeutic treatment of human hepatoma. HDGFs are structurally related to Fibroblast growth factors (Klagsbrun M., Sasse, J., Proc. Natl. Acad. Sci. USA 1986 83(8) 2448-52). This putative growth factor may play an important role in autonomous growth of hepatoma and may lead to useful diagnosis or therapeutic approaches to Human Hepatoma (Nakamura, H., Kambe, H., Egawa, T Clin Chim Acta 1989, 183(3): 273-84). A further embodiment of the invention is the use of SB-HDGF to prevent tumor growth. Inhibition of fibroblast growth factor-2 by the compound Suramin prevents neovascularisation and tumor growth in mice (Pesenti et al., British Journal of Cancer, 66: 367-372.) SBhACRP30a Based on EST expression data, SBHACRP30a is Cancer, obesity, anorexia, primarily or exclusively expressed in heart. Based inflammation , cardiovadcular on the similiarity of SB7HACRP30a ACRP30, disease, growth abnormalities Hib27, C1q complement proteins, TNF, and other members of the TNF superfamily, an embodiment of the invention is the use that the encoded protein of SBhACRP30a may play a role in inflammation, cell proliferation, cell death, immunity, and/or energy homeostatis processes. SBHACRP30a show highest similarity to one member of this superfamily, ACRP30 (Adipocyte Complement-Related Protein of 30 kDa). ACRP30 is made exclusively in adipocytes, and its expression is dysregulated in various forms of obesity (Hu, E, Liang, P and Spiegelman, B M. J. Biol. Chem 271, 10697-10703, 1996). ACRP30 secretion is acutely stimulated by insulin (Scherer, P B, Williams S., Fogliano, M., Baldini, G. and Lodish, J Biol. Chem. 270, 26746- 26749, 1995) and is repressed by chronically elevated levels of insulin. A related molecule, the Hib27 protein from Siberian chipmunks, seems also to be involved in energy homeostasis, as its expression is specifically extinguished during hibernation (Takamatan, N., Ohba, K., Kondo, J., Kondo, N., and Shiba, T. Mol. Cell Biol. 13 1516- 1521, 1993). Recently, it has been shown that the three dimensional structure of ACRP30 is superimposible with that of the TNF's, suggesting that these proteins may have a similar function and mode of action (Shapiro, L and Scherer PB.,. Current Biology 8, 335-338, 1997). TNF's are known to play a role in energy homeostasis, where they are implicated in cachexia, obesity and in insulin resistance (Hotamisligil G S., and Spiegelman B M. Diabetes (1994) 43, 1271-1278; Teoman Uysal K., Wiesbrock S M, Marina M W and Hotamisligil G S, Nature 389, 610-614, 1997). sbg35069DBIa An embodiment of the invention is the use of Anxiety, schizophrenia, feeding sbg35069DBIa to function as a neuropeptide, disorders, anorexia, depression, modulating the activity of the GABA receptor. A grooming, stretching, yawning, simular homologue can displace diazepam from social, sexual and rewarded benzodiazepine (BZD) recognition site on GABA behavior, chronic and acute type A receptors. As such, it may function as a inflammation, cardiovasuclar neuropeptide, modulating the activity of the GABA disease, sleep disorder, learning and receptor (J. B. C. 1986. 261(21): 9727-31). Two forms, memory alteration and altered short and long (Biochem. J. 1995. 306: 327-30), are immune response, cancer, seizure, predicted to be intracellular and secreted, stroke, migraine, asthma, respectively. neuropathy and aging sbg14862SPERCTa An embodiment of the invention is the use of Cancer, infections, autoimmune sbg14862SPERCTa, a secreted protein, in the diseases, wound healing and diagnosis and treatment of cancers. A close homolog hematopoietic disorder of sbg14862SPERCTa is human secreted protein SRCR. sbg24878SIa An embodiment of the invention is the use that the Auto-immune diseases such as encoded protein of sbg24878SIa, a member of the rheumatoid arthritis, systemic immunoglobulin superfamily, may play a roll in cell- lupus erythematosus and tumors cell interactions. The closest homologue to this protein is the mouse sialoadhesin genes, a macrophage sialic acid binding receptor for haemopoietic cells with 17 immunoglobulin-like domains, is proposed to function in both secreted and membrane-bound forms and involved in cell-cell interactions. A further embodiment of the invention is the use of sbg24878SIa to inhibit T-cell-B-cell interactions for treating auto-immune disease such as rheumatoid arthritis, systemic lupus erythematosus etc. Close Homologs of sbg24878SIa are mouse sialoadhesin genes and CD22 beta. sbg34976IGBa An embodiment of the invention is the use of Alzheimers disease, ALS, abnormal sbg34976IGBa, a secreted protein, in the diagnosis keratinocyte differentiation, anti- and treatment of Bardet-Biedl syndrome type 4 thrombosis, atrophia areata, cell (BBS4). A close homolog of sbg34976IGBa is growth, hematopoietic disease, leucine rich repeat (ISLR) mRNA. diseases of the immune system, inflammation, congenital microvillus atrophy, dermal scarring, enterocolitis, cancer, gastrointestinal ulceration, sbg41608HDGFa An embodiment of the invention is the use of Cancer, inflammation, defective sbg41608HDGFa, to control cell growth and immune response, cardiovascular regulation of cell differentiation. Hepatoma-derived disease, growth abnormalities growth factors are members of a diverse family of cytokines. Like other cytokines, they are peptides involved in the control of cell growth, regulation, differentiation and function (e.g. Thomson, The Cytokine Handbook, 2nd edition, Academic Press, Harcourt Brace & co. publishers, London). Another embodiment of the invention is the use of sbg41608HDGFa for diagnosis or therapeutic treatment of human hepatoma. HDGF are structurally related to Fibroblast growth factors (Klagsbrun M., Sasse, I., Proc. Natl. Acad. Sci. USA 1986 83(8) 2448-52). This putative growth factor may play an important role in autonomous growth of hepatoma and may lead to useful diagnosis or therapeutic approaches to Human Hepatoma (Nakamura, H., Kambe, H., Egawa, T Clin Chim Acta 1989, 183(3): 273-84,). A further embodiment of the invention is the use of sbg41608HDGFa to prevent tumor growth. Inhibition of fibroblast growth factor-2 by the compound Surainin prevents neovascularisation and tumor growth in mice (Pesenti et al., British Journal of Cancer, 66: 367- 372) sbg66804SPARCra An embodiment of the invention is the use of Cataractogenesis, angiogenesis, sbg66804SPARCra, in development, remodeling, wound healing, tumors cell turnover, tissue repair, and tumor growth. The closest homologue to this secreted protein is the mouse SPARC-related protein. SPARC (Secreted Protein, Acidic and Rich in Cysteine) is a unique matricellular glycoprotein that is expressed by many different types of cells and is associated with development, remodeling, cell turnover, and tissue repair. Its principal functions in vitro are counteradhesion and antiproliferation, which proceed via different signaling pathways. SPARC has demonstrated activities in angiogenesis, cataractogenesis, and wound healing. SPARC has also been identified in tumors. sbg72825FOLATEa An embodiment of the invention is the use of Epithelial cancers, ovary, uterus sbg72825FOLATEa in the diagnostic and treatment and cervix cancer applications of malignant, such as epithelial cancers, ovary, uterus, cervix cancer and future cancer vaccine developments. A close homolog of sbg72825FOLATEa is membrane bound folate binding protein. SBhPRO221 An embodiment of the invention is the use of Disorders associated with healthy SBhPRO221 in disorders associated with maintanance of gastric mucosa and preservation and maintenance of gastric mucosa, repair of acute and chronic treatment of chronic and acute gastric ulcer, skin mucosal lesion, skin disease, lung disease like epithelial cancer, lung squamous carcinoma, growth abnormalities, carcinoma, neuropathy, Parkinson disease, Parkinson, Alzheimer's dosaes, Alzheimer disease, tissue repair, problems of kidney, ALS, neuropathy and cancer endometrium, blood vessels and other tissue in genital tract. sbg77153CYSa An embodiment of the invention is the use of Tumors and matastasis, sbg77153CYSa in natural tissue remodeling events remodeling bone resorption and such as bone resorption and embryo implantation embryo implantation along with associations with tumor formation and metastasis. The closest homologue is the mouse testatin precursor (Cystatin 9), is related to a group of genes that encodes cysteine protease inhibitors known as cystatins. Cystatins and their target proteases have been associated with tumor formation and metastasis, but also are involved in natural tissue remodeling events such as bone resorption and embryo implantation SBh80014.IAPa An embodiment of the invention is the use of Suppression of apoptosis, cell SBh80014.IAPa in inhibition of apoptosos and thus proliferation, cancer, metastasis, in, cell proliferation, cancer, metastasis, cell death, Inflammation, defective immune immunity, and energy homeostatis processes. A response, growth abnormalities close homolog to SBh80014.IAPa is PIAP (putative inhibitor of apoptosis protein) (C. Steblik et al, Biochem. Biophys. Res. Commun. 243(3), 827-832, 1998). PIAP is made primarlily in tumor cells and is strongly upregulated in response to inflammatory cytokine TNF-•, IL-1 and lipopolysacchrides. The members of this family are conserved across species. sbgFGF-19b An embodiment of the invention is the use of Cerebral ischemia, cancer, sbgFGF-19b in cell growth, regulation, atherosclerosis, rheumatoid arthritis, differentiation, function, angiogenesis, cirrhosis, psoriasis, sarcoidosis, neovascularisation, wound healing, astrogliosis, glial idiopathic pulmonary fibrosis, tumor cell proliferation and differentiation, cerebral development, developmental vasodilation, neurotrophic/neuromodulatory disorders, skeletal disorders, wound processes, improves the outcome in cerebral repair ischemia, promotes neoangiogenesis in ischemic myocardium, and enhances functional recovery and/or promotes neuronal sprouting following focal cerebral infarct. Fibroblast growth factors are a diverse family of cytokines. Like other cytokines, they are peptides involved in the control of cell growth, regulation, differentiation and function (e.g. Thomson, The Cytokine Handbook, 2nd edition, Academic Press, Harcourt Brace & co. publishers, London). Fibroblast growth factors are so called because they are fibroblast mitogens (Gospodarawicz, Journal of Biological Chemistry, (1975) 250: 2515-2520,). Inhibition of fibroblast growth factor-2 by the compound Suramin prevents neovascularisation and tumor growth in mice (Pesenti et al., British Journal of Cancer, 66: 367- 372). Fibroblast growth factors also function in angiogenesis (Lyons, M. K., et al., Brain Res. (1991) 558: 315-320), wound healing (Uhl, E., et al., Br. J. Surg. (1993) 80: 977-980, 1993), astrogliosis, glial cell proliferation and differentiation (Biagini, G. et al., Neurochem. Int. (1994) 25: 17-24), cerebral vasodilation (Tanaka, R. et al., Stroke (1995) 26: 2154-2159), and neurotrophic/neuromodulatory processes. Fibroblast growth factor also has multiple positive effects including blood flow and protection from calcium toxicity to improve outcome in cerebral ischemia (Mattson, M. P. et al., Semin. Neurosci. (1993) 5: 295-307; Doetrocj. W. D. et al., J. Neurotrauma (1996) 13: 309-316). Basic FGF treatment promotes neoangiogenesis in ischemic myocardium (Schumacher et al., Circulation (1998) 97: 645-650). Basic FGF enhances functional recovery and promotes neuronal sprouting following focal cerebral infarct (Kawamata et al., Proc. Natl. Acad. Sci. (1997) 94(15): 8179-84).

[0115] TABLE IV Quantitative, Tissue-specific mRNA expression detected using SybrMan or TaqMan. Quantitative, tissue-specific, mRNA expression patterns of the genes were measured using SYBR-Green Quantitative PCR (Applied Biosystems, Foster City, CA) or TaqMan PCR (Perkin Elmer, see Lie et al. Current Opinion in Biotechnology 9:43-48, 1998; Gibson et al., Genome Methods 6:995-1001, 1996) and human cDNAs prepared from various human tissues. Gene-specific PCR primers were designed using the first nucleic acid sequence listed in the Sequence List for each gene. Results are presented as the number of copies of each specific gene's mRNA detected in 1 ng mRNA pool from each tissue. Two replicate mRNA measurements were made from each tissue RNA. SybrMan Results: Tissue-Specific mRNA Expression (copies per ng mRNA; avg. ± range for 2 data points per tissue) Skeletal Gene name Brain Heart Lung Liver Kidney muscle sbgTango79a 358 ± 7  278 ± 55  239 ± 100  53 ± 20 247 ± 29 461 ± 60 sbgPRO331a 15411 ± 861  1831 ± 25  2409 ± 103 656 ± 2  2283 ± 82  625 ± 47 sbghPYYa −3 ± 1 −1 ± 0  0 ± 0 −7 ± 8  8 ± 2 −5 ± 9 sbghGTa  24 ± 10  5 ± 4  5 ± 3 −4 ± 8  2 ± 1 −3 ± 5 SB-HDGF 4362 ± 359 3387 ± 11  2425 ± 120 972 ± 82 3270 ± 152  7106 ± 1647 SBhACRP30a 10751 ± 954  7443 ± 294 9900 ± 780 6463 ± 45  8530 ± 225 7638 ± 405 sbg35069DBIa 142 ± 15 180 ± 17  94 ± 10 37 ± 3 257 ± 15 73 ± 8 sbg14862SPERCTa 31 ± 3 18 ± 6 23 ± 4 10 ± 6 49 ± 1  8 ± 7 sbg24878SIa 327 ± 29 1251 ± 8  1740 ± 103 552 ± 20  514 ± 182 636 ± 65 sbg34976IGBa 1500 ± 64  451 ± 21 123 ± 14  9 ± 6 55 ± 6 156 ± 6  sbg41608HDGFa 11 ± 4  3 ± 0  4 ± 4  2 ± 0  0 ± 1  1 ± 2 sbg66804SPARCra 296 ± 53 24 ± 0  4 ± 1 457 ± 21  7 ± 0 68 ± 3 sbg72825FOLATEa 289 ± 40 381 ± 12 100 ± 78 92 ± 3  494 ± 102 289 ± 52 SBhPRO221 14 ± 6 109 ± 43 102 ± 30 221 ± 44 19 ± 9  6 ± 5 sbg77153CYSa 50 ± 8  80 ± 32 181 ± 3  10 ± 2 234 ± 50 54 ± 7 SBh80014.IAPa  6 ± 10  82 ± 70 31 ± 3 −2 ± 3 110 ± 1   88 ± 24 sbgFGF-19b  9 ± 9  25 ± 30  8 ± 11  1612 ± 1711  9 ± 16 10 ± 9 Tissue-Specific mRNA Expression (copies per ng mRNA; avg. ± range for 2 data points per tissue) Spleen/ Gene name Intestine lymph Placenta Testis sbgTango79a 83 ± 1 202 ± 18 300 ± 55  770 ± 106 sbgPRO331a 510 ± 5  2096 ± 74  2596 ± 68  4692 ± 472 sbghPYYa −4 ± 1  2 ± 1 −1 ± 0 38 ± 5 sbghGTa −1 ± 3  4 ± 2  4 ± 0 92 ± 8 SB-HDGF 1133 ± 164 2058 ± 101 2528 ± 50  9024 ± 652 SBhACRP30a 6040 ± 438  8912 ± 1021 8931 ± 617 8098 ± 612 sbg35069DBIa  27 ± 10  76 ± 29 184 ± 5  158 ± 2  sbg14862SPERCTa  7 ± 0 23 ± 1 18 ± 2 30 ± 1 sbg24878SIa 582 ± 64 5200 ± 222 5151 ± 271 695 ± 30 sbg34976IGBa  38 ± 12 80 ± 4 76 ± 3 1975 ± 183 sbg41608HDGFa  1 ± 0  7 ± 5  0 ± 0 14909 ± 926  sbg66804SPARCra  9 ± 1 439 ± 11 128 ± 1  1037 ± 17  sbg72825FOLATEa 101 ± 3  219 ± 30  405 ± 121 270 ± 44 SBhPRO221  61 ± 13  60 ± 19  33 ± 11 119 ± 40 sbg77153CYSa 25 ± 8 93 ± 0 151 ± 3  26223 ± 604  SBh80014.IAPa 17 ± 4 29 ± 1 62 ± 3  65 ± 20 sbgFGF-19b  9 ± 15  16 ± 20  0 ± 3  123 ± 144

[0116] TABLE V Additional diseases based on mRNA expression in specific tissues Tissue Expression Additional Diseases Brain Neurological and psychiatric diseases, including Alzheimers, parasupranuclear palsey, Huntington's disease, myotonic dystrophy, anorexia, depression, schizophrenia, headache, amnesias, anxiety disorders, sleep disorders, multiple sclerosis Heart Cardiovascular diseases, including congestive heart failure, dilated cardiomyopathy, cardiac arrhythmias, Hodgson's Disease, myocardial infarction, cardiac arrhythmias Lung Respiratory diseases, including asthma, Chronic Obstructive Pulmonary Disease, cystic fibrosis, acute bronchitis, adult respiratory distress syndrome Liver Dyslipidemia, hypercholesterolemia, hypertriglyceridemia, cirrhosis, hepatic encephalopathy, fatty hepatocirrhosis, viral and nonviral hepatitis, Type II Diabetes Mellitis, impaired glucose tolerance Kidney Renal diseases, including acute and chronic renal failure, acute tubular necrosis, cystinuria, Fanconi's Syndrome, glomerulonephritis, renal cell carcinoma, renovascular hypertension Skeletal muscle Eulenburg's Disease, hypoglycemia, obesity, tendinitis, periodic paralyses, malignant hyperthermia, paramyotonia congenita, myotonia congenita Intestine Gastrointestinal diseases, including Myotonia congenita, Ileus, Intestinal Obstruction, Tropical Sprue, Pseudomembranous Enterocolitis Spleen/lymph Lymphangiectasia, hypersplenism, angiomas, ankylosing spondylitis, Hodgkin's Disease, macroglobulinemia, malignant lymphomas, rheumatoid arthritis Placenta Choriocarcinoma, hydatidiform mole, placenta previa Testis Testicular cancer, male reproductive diseases, including low testosterone and male infertility Pancreas Diabetic ketoacidosis, Type 1 & 2 diabetes, obesity, impaired glucose tolerance

[0117]

1 46 1 1779 DNA Homo sapiens 1 atgacctgct ggctgtgcgt cctgagcctg cccctgctcc tgctgcccgc ggcgccgccc 60 ccggctggag gctgcccggc ccgctgcgag tgcaccgtgc agacccgcgc ggtggcctgc 120 acgcgccgcc gcctgaccgc cgtgcccgac ggcatcccgg ccgagacccg cctgctggag 180 ctcagccgca accgcatccg ctgcctgaac ccgggcgacc tggccgcgct gcccgcgctg 240 gaggagctgg acctgagcga gaacgccatc gcgcacgtgg agcccggcgc cttcgccaac 300 ctgccgcgcc tgcgcgtcct gcgtctccgt ggcaaccagc tgaagctcat cccgcccggg 360 gtcttcacgc gcctggacaa cctcacgctg ctggacctga gcgagaacaa gctggtaatc 420 ctgctggact acactttcca ggacctgcac agcctgcgcc ggctggaagt gggcgacaac 480 gacctggtat tcgtctcgcg ccgcgccttc gcggggctgc tggccctgga ggagctgacc 540 ctggagcgct gcaacctcac ggctctgtcc ggggagtcgc tgggccatct gcgcagcctg 600 ggcgccctgc ggctgcgcca cctggccatc gcctccctgg aggaccagaa cttccgcagg 660 ctgcccgggc tgctgcacct ggagattgac aactggccgc tgctggagga ggtggcggcg 720 ggcagcctgc ggggcctgaa cctgacctcg ctgtcggtca cccacaccaa catcaccgcc 780 gtgccggccg ccgcgctgcg gcaccaggcg cacctcacct gcctcaatct gtcgcacaac 840 cccatcagca cggtgccgcg ggggtcgttc cgggacctgg tccgcctgcg cgagctgcac 900 ctggccgggg ccctgctggc tgtggtggag ccgcaggcct tcctgggcct gcgccagatc 960 cgcctgctca acctctccaa caacctgctc tccacgttgg aggagagcac cttccactcg 1020 gtgaacacgc tagagacgct gcgcgtggac gggaacccgc tggcctgcga ctgtcgcctg 1080 ctgtggatcg tgcagcgtcg caagaccctc aacttcgacg ggcggctgcc ggcctgcgcc 1140 accccggccg aggtgcgcgg cgacgcgctg cgaaacctgc cggactccgt gctgttcgag 1200 tacttcgtgt gccgcaaacc caagatccgg gagcggcggc tgcagcgcgt cacggccacc 1260 gcgggcgaag acgtccgctt cctctgccgc gccgagggcg agccggcgcc caccgtggcc 1320 tgggtgaccc cccagcaccg gccggtgacg gccaccagcg cgggccgggc gcgcgtgctc 1380 cccgggggga cgctggagat ccaggacgcg cggccgcagg acagcggcac ctacacgtgc 1440 gtggccagca acgcgggcgg caacgacacc tacttcgcca cgctgaccgt gcgccccgag 1500 ccggccgcca accggacccc gggcgaggcc cacaacgaga cgctggcggc cctgcgcgcg 1560 ccgctcgacc tcaccaccat cctggtgtcc accgccatgg gctgcatcac cttcctgggc 1620 gtggtcctct tctgcttcgt gctgctgttc gtgtggagcc gcggccgcgg gcagcacaaa 1680 aacaacttct cggtggagta ctccttccgc aaggtggatg ggccggccgc cgcggcgggc 1740 cagggaggcg cgcgcaagtt caacatgaag atgatctga 1779 2 1962 DNA Homo sapiens 2 atgaagctct tgtggcaggt aactgtgcac caccacacct ggaatgccat cctgctcccg 60 ttcgtctacc tcacggcgca agtgtggatt ctgtgtgcag ccatcgctgc tgccgcctca 120 gccgggcccc agaactgccc ctccgtctgc tcgtgcagta accagttcag caaggtggtg 180 tgcacgcgcc ggggcctctc cgaggtcccg cagggtattc cctcgaacac ccggtacctc 240 aacctcatgg agaacaacat ccagatgatc caggccgaca ccttccgcca cctccaccac 300 ctggaggtcc tgcagttggg caggaactcc atccggcaga ttgaggtggg ggccttcaac 360 ggcctggcca gcctcaacac cctggagctg ttcgacaact ggctgacagt catccctagc 420 ggggcctttg aatacctgtc caagctgcgg gagctctggc ttcgcaacaa ccccatcgaa 480 agcatcccct cttacgcctt caaccgggtg ccctccctca tgcgcctgga cttgggggag 540 ctcaagaagc tggagtatat ctctgaggga gcttttgagg ggctgttcaa cctcaagtat 600 ctgaacttgg gcatgtgcaa cattaaagac atgcccaatc tcacccccct ggtggggctg 660 gaggagctgg agatgtcagg gaaccacttc cctgagatca ggcctggctc cttccatggc 720 ctgagctccc tcaagaagct ctgggtcatg aactcacagg tcagcctgat tgagcggaat 780 gcttttgacg ggctggcttc acttgtggaa ctcaacttgg cccacaataa cctctcttct 840 ttgccccatg acctctttac cccgctgagg tacctggtgg agttgcatct acaccacaac 900 ccttggaact gtgattgtga cattctgtgg ctagcctggt ggcttcgaga gtatataccc 960 accaattcca cctgctgtgg ccgctgtcat gctcccatgc acatgcgagg ccgctacctc 1020 gtggaggtgg accaggcctc cttccagtgc tctgccccct tcatcatgga cgcacctcga 1080 gacctcaaca tttctgaggg tcggatggca gaacttaagt gtcggactcc ccctatgtcc 1140 tccgtgaagt ggttgctgcc caatgggaca gtgctcagcc acgcctcccg ccacccaagg 1200 atctctgtcc tcaacgacgg caccttgaac ttttcccacg tgctgctttc agacactggg 1260 gtgtacacat gcatggtgac caatgttgca ggcaactcca acgcctcggc ctacctcaat 1320 gtgagcacgg ctgagcttaa cacctccaac tacagcttct tcaccacagt aacagtggag 1380 accacggaga tctcgcctga ggacacaacg cgaaagtaca agcctgttcc taccacgtcc 1440 actggttacc agccggcata taccacctct accacggtgc tcattcagac tacccgtgtg 1500 cccaagcagg tggcagtacc cgcgacagac accactgaca agatgcagac cagcctggat 1560 gaagtcatga agaccaccaa gatcatcatt ggctgctttg tggcagtgac tctgctagct 1620 gccgccatgt tgattgtctt ctataaactt cgtaagcggc accagcagcg gagtacagtc 1680 acagccgccc ggactgttga gataatccag gtggacgaag acatcccagc agcaacatcc 1740 gcagcagcaa cagcagctcc gtccggtgta tcaggtgagg gggcagtagt gctgcccaca 1800 attcatgacc atattaacta caacacctac aaaccagcac atggggccca ctggacagaa 1860 aacagcctgg ggaactctct gcaccccaca gtcaccacta tctctgaacc ttatataatt 1920 cagacccata ccaaggacaa ggtacaggaa actcaaatat ga 1962 3 213 DNA Homo sapiens 3 atggtgtcgg tgtgcaggcc gtggcctgct gtggccatag cacttctggc tctgctggtc 60 tgcctggggg cgctggtcga cacctgcccc atcaaacccg aggctcctgg cgaagacgag 120 tccctggagg agctgagcca ctattatgct tccctgtgcc actacctcaa cgtggtcacc 180 agacagtggt gggagggtgc agacatgtgg tga 213 4 393 DNA Homo sapiens 4 atgaagctgg cattcctctt ccttggcccc atggccctcc tccttctggc tggctatggc 60 tgtgtcctcg gtgcctccag tgggaacctg cgcacctttg tgggctgtgc cgtgagggag 120 tttactttcc tggccaagaa gccaggctgc aggggccttc ggatcaccac ggatgcctgc 180 tggggtcgct gtgagacctg ggagaaaccc attctggaac ccccctatat tgaagcccat 240 catcgagtct gtacctacaa cgagaccaaa caggtgactg tcaagctgcc caactgtgcc 300 ccgggagtcg accccttcta cacctatccc gtggccatcc gctgtgactg cggagcctgc 360 tccactgcca ccacggagtg tgagaccatc tga 393 5 2031 DNA Homo sapiens 5 attccaaacg cctttaaacc cggggacttg gttttcccta aaattaaggg ctaccctcaa 60 tggccttcca ggatcgacga catcgcggat ggcgccgtga agcccccacc caacaagtac 120 cccatctttt tctttggcac acacgaaaca gccttcctgg gacccaagga cctgttcccc 180 tacgacaaat gtaaagacaa gtacgggaag cccaacaaga ggaaaggctt caatgaaggg 240 ctgtgggaga tccagaacaa cccccacgcc agctacagcg cccctccgcc agtgagctcc 300 tccgacagcg aggcccccga ggccaacccc gccgacggca gtgacgctga cgaggacgat 360 gaggaccggg gggtcatggc cgtcacagcg gtaaccgcca cagctgccag cgacaggatg 420 gagagcgact cagactcaga caagagtagc gacaacagtg gcctgaagag gaagacgcct 480 gcgctaaaga tgtcggtctc gaaacgagcc cgaaaggcct ccagcgacct ggatcaggcc 540 agcgtgtccc catccgaaga ggagaactcg gaaagctcat ctgagtcgga gaagaccagc 600 gaccaggact tcacacctga gaagaaagca gcggtccggg cgccacggag gggccctctg 660 gggggacgga aaaaaaagaa ggcgccatca gcctccgact ccgactccaa ggccgattcg 720 gacggggcca agcctgagcc ggtggccatg gcgcggtcgg cgtcctcctc ctcctcttcc 780 tcctcctcct ccgactccga tgtgtctgtg aagaagcctc cgaggggcag gaagccagcg 840 gagaagcctc tcccgaagcc gcgagggcgg aaaccgaagc ctgaacggcc tccgtccagc 900 tccagcagtg acagtgacag cgacgaggtg gaccgcatca gtgagtggaa gcggcgggac 960 gaggcgcgga ggcgcgagct ggaggcccgg cggcggcgag agcaggagga ggagctgcgg 1020 cgcctgcggg agcaggagaa ggaggagaag gagcggaggc gcgagcgggc cgaccgcggg 1080 gaggctgagc ggggcagcgg cggcagcagc ggggacgagc tcagggagga cgatgagccc 1140 gtcaagaagc ggggacgcaa gggccggggc cggggtcccc cgtcctcctc tgactccgag 1200 cccgaggccg agctggagag agaggccaag aaatcagcga agaagccgca gtcctcaagc 1260 acagagcccg ccaggaaacc tggccagaag gagaagagag tgcggcccga ggagaagcaa 1320 caagccaagc ccgtgaaggt ggagcggacc cggaagcggt ccgagggctt ctcgatggac 1380 aggaaggtag agaagaagaa agagccctcc gtggaggaga agctgcagaa gctgcacagt 1440 gagatcaagt ttgccctaaa ggtcgacagc ccggacgtga agaggtgcct gaatgcccta 1500 gaggagctgg gaaccctgca ggtgacctct cagatcctcc agaagaacac agacgtggtg 1560 gccaccttga agaagattcg ccgttacaaa gcgaacaagg acgtaatgga gaaggcagca 1620 gaagtctata cccggctcaa gtcgcgggtc ctcggcccaa agatcgaggc ggtgcagaaa 1680 gtgaacaagg ctgggatgga gaaggagaag gccgaggaga agctggccgg ggaggagctg 1740 gccggggagg agctggccgg ggaggaggcc ccccaggaga aggcggagga caagcccagc 1800 accgatctct cagccccagt gaatggcgag gccacatcac agaaggggga gagcgcagag 1860 gacaaggagc acgaggaggg tcgggactcg gaggaggggc caaggtgtgg ctcctctgaa 1920 gacctgcacg acagcgtacg ggagggtccc gacctggaca ggcctgggag cgaccggcag 1980 gagcgcgaga gggcacgggg ggactcggag gccctggacg aggagagctg a 2031 6 2154 DNA Homo sapiens 6 atggcggtcc tggacctgag ggagctgcgc cgtggggatc tggggggtgt ccagggcctg 60 aaggagctgc ggcgccaatg gtctgggggt cctgggcctg aggaagctgc gctctggggg 120 tctggggctt ctgtgcctga gggagctgca ccatggggat ctggggttgc cctggcccag 180 agggagccac gcctcatcga cgacatcgcg gatggcgccg tgaagccccc acccaacaag 240 taccccatct ttttctttgg cacacacgaa acagccttcc tgggacccaa ggacctgttc 300 ccctacgaca aatgtaaaga caagtacggg aagcccaaca agaggaaagg cttcaatgaa 360 gggctgtggg agatccagaa caacccccac gccagctaca gcgcccctcc gccagtgagc 420 tcctccgaca gcgaggcccc cgaggccaac cccgccgacg gcagtgacgc tgacgaggac 480 gatgaggacc ggggggtcat ggccgtcaca gcggtaaccg ccacagctgc cagcgacagg 540 atggagagcg actcagactc agacaagagt agcgacaaca gtggcctgaa gaggaagacg 600 cctgcgctaa agatgtcggt ctcgaaacga gcccgaaagg cctccagcga cctggatcag 660 gccagcgtgt ccccatccga agaggagaac tcggaaagct catctgagtc ggagaagacc 720 agcgaccagg acttcacacc tgagaagaaa gcagcggtcc gggcgccacg gaggggccct 780 ctggggggac ggaaaaaaaa gaaggcgcca tcagcctccg actccgactc caaggccgat 840 tcggacgggg ccaagcctga gccggtggcc atggcgcggt cggcgtcctc ctcctcctct 900 tcctcctcct cctccgactc cgatgtgtct gtgaagaagc ctccgagggg caggaagcca 960 gcggagaagc ctctcccgaa gccgcgaggg cggaaaccga agcctgaacg gcctccgtcc 1020 agctccagca gtgacagtga cagcgacgag gtggaccgca tcagtgagtg gaagcggcgg 1080 gacgaggcgc ggaggcgcga gctggaggcc cggcggcggc gagagcagga ggaggagctg 1140 cggcgcctgc gggagcagga gaaggaggag aaggagcgga ggcgcgagcg ggccgaccgc 1200 ggggaggctg agcggggcag cggcggcagc agcggggacg agctcaggga ggacgatgag 1260 cccgtcaaga agcggggacg caagggccgg ggccggggtc ccccgtcctc ctctgactcc 1320 gagcccgagg ccgagctgga gagagaggcc aagaaatcag cgaagaagcc gcagtcctca 1380 agcacagagc ccgccaggaa acctggccag aaggagaaga gagtgcggcc cgaggagaag 1440 caacaagcca agcccgtgaa ggtggagcgg acccggaagc ggtccgaggg cttctcgatg 1500 gacaggaagg tagagaagaa gaaagagccc tccgtggagg agaagctgca gaagctgcac 1560 agtgagatca agtttgccct aaaggtcgac agcccggacg tgaagaggtg cctgaatgcc 1620 ctagaggagc tgggaaccct gcaggtgacc tctcagatcc tccagaagaa cacagacgtg 1680 gtggccacct tgaagaagat tcgccgttac aaagcgaaca aggacgtaat ggagaaggca 1740 gcagaagtct atacccggct caagtcgcgg gtcctcggcc caaagatcga ggcggtgcag 1800 aaagtgaaca aggctgggat ggagaaggag aaggccgagg agaagctggc cggggaggag 1860 ctggccgggg aggagctggc cggggaggag gccccccagg agaaggcgga ggacaagccc 1920 agcaccgatc tctcagcccc agtgaatggc gaggccacat cacagaaggg ggagagcgca 1980 gaggacaagg agcacgagga gggtcgggac tcggaggagg ggccaaggtg tggctcctct 2040 gaagacctgc acgacagcgt acgggagggt cccgacctgg acaggcctgg gagcgaccgg 2100 caggagcgcg agagggcacg gggggactcg gaggccctgg acgaggagag ctga 2154 7 870 DNA Homo sapiens 7 atgtttgtct tgctctatgt tacaagtttt gccatttgtg ccagtggaca accccggggt 60 aatcagttga aaggagagaa ctactccccc aggtatatct gcagcattcc tggcttgcct 120 ggacctccag ggccccctgg agcaaatggt tcccctgggc cccatggtcg catcggcctt 180 ccaggaagag atggtagaga cggcaggaaa ggagagaaag gtgaaaaggg aactgcaggt 240 ttgagaggta agactggacc gctaggtctt gccggtgaga aaggggacca aggagagact 300 gggaagaaag gacccatagg accagaggga gagaaaggag aagtaggtcc aattggtcct 360 cctggaccaa agggagacag aggagaacaa ggggacccgg ggctgcctgg agtttgcaga 420 tgtggaagca tcgtgctcaa atccgccttt tctgttggca tcacaaccag ctacccagaa 480 gaaagactac ctattatatt taacaaggtc ctcttcaacg agggagagca ctacaaccct 540 gccacaggga agttcatctg tgctttccca gggatctatt acttttctta tgatatcaca 600 ttggctaata agcatctggc aatcggactg gtacacaatg ggcaataccg gataaagacc 660 ttcgacgcca acacaggaaa ccatgatgtg gcttcggggt ccacagtcat ctatctgcag 720 ccagaagatg aagtctggct ggagattttc ttcacagacc agaatggcct cttctcagac 780 ccaggttggg cagacagctt attctccggg tttctcttat acgttgacac agattaccta 840 gattccatat cagaagatga tgaattgtga 870 8 912 DNA Homo sapiens 8 atggggaagg aggacactca agaaactcgc acagagccaa agatgtttgt cttgctctat 60 gttacaagtt ttgccatttg tgccagtgga caaccccggg gtaatcagtt gaaaggagag 120 aactactccc ccaggtatat ctgcagcatt cctggcttgc ctggacctcc agggccccct 180 ggagcaaatg gttcccctgg gccccatggt cgcatcggcc ttccaggaag agatggtaga 240 gacggcagga aaggagagaa aggtgaaaag ggaactgcag gtttgagagg taagactgga 300 ccgctaggtc ttgccggtga gaaaggggac caaggagaga ctgggaagaa aggacccata 360 ggaccagagg gagagaaagg agaagtaggt ccaattggtc ctcctggacc aaagggagac 420 agaggagaac aaggggaccc ggggctgcct ggagtttgca gatgtggaag catcgtgctc 480 aaatccgcct tttctgttgg catcacaacc agctacccag aagaaagact acctattata 540 tttaacaagg tcctcttcaa cgagggagag cactacaacc ctgccacagg gaagttcatc 600 tgtgctttcc cagggatcta ttacttttct tatgatatca cattggctaa taagcatctg 660 gcaatcggac tggtacacaa tgggcaatac cggataaaga ccttcgacgc caacacagga 720 aaccatgatg tggcttcggg gtccacagtc atctatctgc agccagaaga tgaagtctgg 780 ctggagattt tcttcacaga ccagaatggc ctcttctcag acccaggttg ggcagacagc 840 ttattctccg ggtttctctt atacgttgac acagattacc tagattccat atcagaagat 900 gatgaattgt ga 912 9 267 DNA Homo sapiens 9 atgtccctgc aggctgattt tgacatggtc acagaagatg tgaggaagct gaaaacaaga 60 ccagatgatg aagaactgaa agaactttat gggctttaca aacaagctgt aattggaaac 120 attaatattg agtgttcaga aatgctagaa ttaaaaggca aggccaaatg ggaagcacag 180 aacccccaaa aaggattgtc agaggaagat atgatgcgtg cctttatttc taaagccgaa 240 gagctgatag aaaaatatgg aatttag 267 10 1269 DNA Homo sapiens 10 atgcacggtg gctcctgggg cagcgtctgt gatgacgact gggacgtggt ggacgccaac 60 gtagtgtgtc gccagctggg ctgtggcctg gcactgcccg tgccacggcc ccttgccttt 120 ggccaaggcc gaggccccat cctgctggac aacgtggagt gccgcgggca ggaagctgcg 180 ctgagcgagt gcggcagccg cggctggggc gtccacaatt gctttcacta cgaggatgtg 240 gctgtcctgt gtgatggtga gggcagcgta cgcctggtag ggggcgcgaa cctgtgtcag 300 ggccgagtgg agatcctgca cagtggcctg tggggcaccg tgtgtgacga cgactggggg 360 ctgccggatg ccgctgtggt ctgtcgtcag ctgggctgcg gggcggccat ggccgccacc 420 accaacgcct tcttcggcta tggcaccgga cacatcctgc tggacaacgt gcactgcgaa 480 ggcggcgagc cccgcctggc agcctgccag agcctgggct ggggtgtgca caactgcggc 540 caccacgagg acgcgggcgc gctctgcgca ggtgcgggct ctaggggcga tgggcggggc 600 cggggcagcc cctctggccg cgggcctgtg cgccccgcag gtggacggct gcgactggtg 660 ggcggcccgg gtccgtgccg cggccgcgtg gaggtgttgc acgccggggg ctggggcacc 720 gtgtgcgacg atgactggga ctttgcggac gcgcgcgtgg cctgccgcga agcgggctgc 780 gggcctgcgc tgggcgctac gggactgggc cacttcggct acggccgcgg ccccgtgctg 840 ctggacaacg tgggctgcgc cggcaccgag gctcgcctga gcgactgctt ccacctgggc 900 tggggccagc acaactgcgg ccaccacgag gacgcgggag cgctctgcgc agggcatcta 960 cgtctggtca atggagccca ccgatgcgag ggacgtgtag agctctacct agggcaacgg 1020 tggggcactg tctgtgatga tgcttgggac ctgcgggcag ccggtgtcct gtgccgccag 1080 ctgggctgtg gccaggccct cgcagcccct ggcgaggctc actttggccc aggccgaggc 1140 cccattctcc tggacaatgt caagtgccgt ggggaagaaa gtgctctgct gctctgctct 1200 catatccgct gggatgccca caactgtgac cacagcgagg atgccagtgt cctgtgccag 1260 ccttcatga 1269 11 1659 DNA Homo sapiens 11 atggccacat taccagagaa ggccctgaaa gaggcctgga agggattgat cccaaggttc 60 ccatggcttc atggcaaagc ggagctgagg ctggtggggg gccccagccg ctgccggggc 120 cgcctggaag tcatgcacgg tggctcctgg ggcagcgtct gtgatgacga ctgggacgtg 180 gtggacgcca acgtagtgtg tcgccagctg ggctgtggcc tggcactgcc cgtgccacgg 240 ccccttgcct ttggccaagg ccgaggcccc atcctgctgg acaacgtgga gtgccgcggg 300 caggaagctg cgctgagcga gtgcggcagc cgcggctggg gcgtccacaa ttgctttcac 360 tacgaggatg tggctgtcct gtgtgatgaa ttcttgccaa cgcagccccc aacaaggaag 420 atgttaacca gtagagcacc tcctacgaca ctgccgaatg gaaaaagtga gggcagcgta 480 cgcctggtag ggggcgcgaa cctgtgtcag ggccgagtgg agatcctgca cagtggcctg 540 tggggcaccg tgtgtgacga cgactggggg ctgccggatg ccgctgtggt ctgtcgtcag 600 ctgggctgcg gggcggccat ggccgccacc accaacgcct tcttcggcta tggcaccgga 660 cacatcctgc tggacaacgt gcactgcgaa ggcggcgagc cccgcctggc agcctgccag 720 agcctgggct ggggtgtgca caactgcggc caccacgagg acgcgggcgc gctctgcgca 780 ggcctgggtc ccccaacgct cacagcactg ccatcctcag ccacaagaga ggactgggct 840 tggcagacag atccgtccgc tacaggagtt ggcccccagc cttcccggga gacagcactg 900 ctcaccaccg ccgcctgggc cgcggggaag aaaagtggac ggctgcgact ggtgggcggc 960 ccgggtccgt gccgcggccg cgtggaggtg ttgcacgccg ggggctgggg caccgtgtgc 1020 gacgatgact gggactttgc ggacgcgcgc gtggcctgcc gcgaagcggg ctgcgggcct 1080 gcgctgggcg ctacgggact gggccacttc ggctacggcc gcggccccgt gctgctggac 1140 aacgtgggct gcgccggcac cgaggctcgc ctgagcgact gcttccacct gggctggggc 1200 cagcacaact gcggccacca cgaggacgcg ggagcgctct gcgcaggtga ggctgacagc 1260 gaaggcccag aggagctggg actgcaagtc cagcaggatg gttctgagac cacgcgggtg 1320 cccactcctc ggcccaggga cgggcatcta cgtctggtca atggagccca ccgatgcgag 1380 ggacgtgtag agctctacct agggcaacgg tggggcactg tctgtgatga tgcttgggac 1440 ctgcgggcag ccggtgtcct gtgccgccag ctgggctgtg gccaggccct cgcagcccct 1500 ggcgaggctc actttggccc aggccgaggc cccattctcc tggacaatgt caagtgccgt 1560 ggggaagaaa gtgctctgct gctctgctct catatccgct gggatgccca caactgtgac 1620 cacagcgagg atgccagtgt cctgtgccag ccttcatga 1659 12 5130 DNA Homo sapiens 12 tgggcttct tgcccaagct tctcctcctg gcctcattct tcccagcagg ccaggcctca 60 tggggcgtct ccagtcccca ggacgtgcag ggtgtgaagg ggtcttgcct gcttatcccc 120 tgcatcttca gcttccctgc cgacgtggag gtgcccgacg gcatcacggc catctggtac 180 tacgactact cgggccagcg gcaggtggtg agccactcgg cggaccccaa gctggtggag 240 gcccgcttcc gcggccgcac cgagttcatg gggaaccccg agcacagggt gtgcaacctg 300 ctgctgaagg acctgcagcc cgaggactct ggttcctaca acttccgctt cgagatcagt 360 gaggtcaacc gctggtcaga tgtgaaaggc accttggtca cagtaacaga ggagcccagg 420 gtgcccacca ttgcctcccc ggtggagctt ctcgagggca cagaggtgga cttcaactgc 480 tccactccct acgtatgcct gcaggagcag gtcagactgc agtggcaagg ccaggaccct 540 gctcgctctg tcaccttcaa cagccagaag tttgagccca ccggcgtcgg ccacctggag 600 accctccaca tggccatgtc ctggcaggac cacggccgga tcctgcgctg ccagctctcc 660 gtggccaatc acagggctca gagcgagatt cacctccaag tgaagtatgc ccccaagggt 720 gtgaagatcc tcctcagccc ctcggggagg aacatccttc caggtgagct ggtcacactc 780 acctgccagg tgaacagcag ctaccctgca gtcagttcca ttaagtggct caaggatggg 840 gtacgcctcc aaaccaagac tggtgtgctg cacctgcccc aggcagcctg gagcgatgct 900 ggcgtctaca cctgccaagc tgagaacggc gtgggctctt tggtctcacc ccccatcagc 960 ctccacatct tcatggctga ggtccaggtg agcccagcag gtcccatcct ggagaaccag 1020 acagtgacac tagtctgcaa cacacccaat gaggcaccca gtgatctccg ctacagctgg 1080 tacaagaacc atgtcctgct ggaggatgcc cactcccata ccctccggct gcacttggcc 1140 actagggctg atactggctt ctacttctgt gaggtgcaga acgtccatgg cagcgagcgc 1200 tcgggccctg tcagcgtggt agtcaacctc ctgacagcct tcctggagac ccaggcggga 1260 cttgtgggca tccttcactg ctctgtggtc agtgagcccc tggccacact ggtgctgtca 1320 catgggggtc atatcctggc ctccacctcc ggggacagtg atcacagccc acgcttcagt 1380 ggtacctctg gtcccaactc cctgcgcctg gagatccgag acctggagga aactgacagt 1440 ggggagtaca agtgctcagc caccaactcc cttggaaatg caacctccac cctggacttc 1500 catgccaatg ccgcccgtct cctcatcagc ccggcagccg aggtggtgga aggacaggca 1560 gtgacactga gctgcagaag cggcctaagc cccacacctg atgcccgctt ctcctggtac 1620 ctgaatggag ccctgcttca cgagggtccc ggcagcagcc tcctgctccc cgcggcctcc 1680 agcactgacg ccggctcata ccactgccgg gcccgggacg gccacagtgc cagtggcccc 1740 tcttcgccag ctgttctcac tgtgctctac ccccctcgac aaccaacatt caccaccagg 1800 ctggaccttg atgccgctgg ggccggggct ggacggcgag gcctcctttt gtgccgtgtg 1860 gacagcgacc cccccgccag gctgcagctg ctccacaagg accgtgttgt ggccacttcc 1920 ctgccatcag ggggtggctg cagcacctgt gggggctgtt ccccacgcat gaaggtcacc 1980 aaagccccca acttgctgcg tgtggagatt cacaaccctt tgctggaaga ggagggcttg 2040 tacctctgtg aggccagcaa tgccctgggc aacgcctcca cctcagccac cttcaatggc 2100 caggccactg tcctggccat tgcaccatca cacacacttc aggagggcac agaagccaac 2160 ttgacttgca acgtgagccg ggaagctgct ggcagccctg ctaacttctc ctggttccga 2220 aatggggtgc tgtgggccca gggtcccctg gagaccgtga cactgctgcc cgtggccaga 2280 actgatgctg ccctttacgc ctgccgcatc ctgactgagg ctggtgccca gctctccact 2340 cccgtgctcc tgagtgtact ctatcccccg gaccgtccaa agctgtcagc cctcctagac 2400 atgggccagg gccacatggc tctgttcatc tgcactgtgg acagccgccc cctggccttg 2460 ctggccttgt tccatgggga gcacctcctg gccaccagcc tgggtcccca ggtcccatcc 2520 catggtcggt tccaggctaa agctgaggcc aactccctga agttagaggt ccgagaactg 2580 ggccttgggg actctggcag ctaccgctgt gaggccacaa atgttcttgg atcatccaac 2640 acctcactct tcttccaggt ccgaggagcc tgggtccagg tgtcaccatc acctgagctc 2700 caagagggcc aggctgtggt cctgagctgc caggtacaca caggagtccc agaggggacc 2760 tcatatcgtt ggtatcggga tggccagccc ctccaggagt cgacctcggc cacgctccgc 2820 tttgcagcca taactttgac acaagctggg gcctatcatt gccaagccca ggccccaggc 2880 tcagccacca cgagcctagc tgcacccatc agcctccacg tgtcctatgc cccacgccac 2940 gtcacactca ctaccctgat ggacacaggc cctggacgac tgggcctcct cctgtgccgt 3000 gtggacagtg accctccggc ccagctgcgg ctgctccacg gggatcgcct tgtggcctcc 3060 accctacaag gtgtgggggg acccgaaggc agctctccca ggctgcatgt ggctgtggcc 3120 cccaacacac tgcgtctgga gatccacggg gctatgctgg aggatgaggg tgtctatatc 3180 tgtgaggcct ccaacaccct gggccaggcc tcggcctcag ctgacttcga cgctcaagct 3240 gtgaatgtgc aggtgtggcc cggggctacc gtgcgggagg ggcagctggt gaacctgacc 3300 tgccttgtgt ggaccactca cccggcccag ctcacctaca catggtacca ggatgggcag 3360 cagcgcctgg atgcccactc catccccctg cccaacgtca cagtcaggga tgccacctcc 3420 taccgctgcg gtgtgggccc ccctggtcgg gcaccccgcc tctccagacc tatcaccttg 3480 gacgtcctct acgcgccccg caacctgcgc ctgacctacc tcctggagag ccatggcggg 3540 cagctggccc tggtactgtg cactgtggac agccgcccgc ccgcccagct ggccctcagc 3600 cacgccggtc gcctcttggc ctcctcgaca gcagcctctg tccccaacac cctgcgcctg 3660 gagctgcgag ggccacagcc cagggatgag ggtttctaca gctgctctgc ccgcagccct 3720 ctgggccagg ccaacacgtc cctggagctg cggctggagg gtgtgcgggt gatcctggct 3780 ccggaggctg ccgtgcctga aggtgccccc atcacagtga cctgtgcgga ccctgctgcc 3840 cacgcaccca cactctatac ttggtaccac aacggtcgtt ggctgcagga gggtccagct 3900 gcctcactct cattcctggt ggccacgcgg gctcatgcag gcgcctactc ttgccaggcc 3960 caggatgccc agggcacccg cagctcccgt cctgctgccc tgcaagtcct ctatgcccct 4020 caggacgctg tcctgtcctc cttccgggac tccagggcca gatccatggc tgtgatacag 4080 tgcactgtgg acagtgagcc acctgctgag ctggccctat ctcatgatgg caaggtgctg 4140 gccacgagca gcggggtcca cagcttggca tcagggacag gccatgtcca ggtggcccga 4200 aacgccctac ggctgcaggt gcaagatgtg cctgcaggtg atgacaccta tgtttgcaca 4260 gcccaaaact tgctgggctc aatcagcacc atcgggcggt tgcaggtaga aggtgcacgc 4320 gtggtggcag agcctggcct ggacgtgcct gagggcgctg ccctgaacct cagctgccgc 4380 ctcctgggtg gccctgggcc tgtgggcaac tccacctttg catggttctg gaatgaccgg 4440 cggctgcacg cggagcctgt gcccactctc gccttcaccc acgtggctcg tgctcaagct 4500 gggatgtacc actgcctggc tgagctcccc actggggctg ctgcctctgc tccagtcatg 4560 ctccgtgtgc tctaccctcc caagacgccc accatgatgg tcttcgtgga gcctgagggt 4620 ggcctccggg gcatcctgga ttgccgagtg gacagcgagc cgctcgccag cctgactctc 4680 caccttggca gtcgactggt ggcctccagt cagccccagg gtgctcctgc agagccacac 4740 atccatgtcc tggcttcccc caatgccctg agggtggaca tcgaggcgct gaggcccagc 4800 gaccaagggg aatacatctg ttctgcctca aatgtcctgg gctctgcctc tacctccacc 4860 tactttgggg tcagagccct gcaccgcctg catcagttcc agcagctgct ctgggtcctg 4920 ggactgctgg tgggcctcct gctcctgctg ttgggcctgg gggcctgcta cacctggaga 4980 aggaggcgtg tttgtaagca gagcatgggc gagaattcgg tggagatggc ttttcagaaa 5040 gagaccacgc agggttttct ctgtgggaag ctcattgatc ctgatgcagc cacatgtgag 5100 acctcaacct gtgccccacc cctgggctga 5130 13 5158 DNA Homo sapiens 13 atgggcttct tgcccaagct tctcctcctg gcctcattct tcccagcagg ccaggcctca 60 tggggcgtct ccagtcccca ggacgtgcag ggtgtgaagg ggtcttgcct gcttatcccc 120 tgcatcttca gcttccctgc cgacgtggag gtgcccgacg gcatcacggc catctggtac 180 tacgactact cgggccagcg gcaggtggtg agccactcgg cggaccccaa gctggtggag 240 gcccgcttcc gcggccgcac cgagttcatg gggaaccccg agcacagggt gtgcaacctg 300 ctgctgaagg acctgcagcc cgaggactct ggttcctaca acttccgctt cgagatcagt 360 gaggtcaacc gctggtcaga tgtgaaaggc accttggtca cagtaacaga ggagcccagg 420 gtgcccacca ttgcctcccc ggtggagctt ctcgagggca cagaggtgga cttcaactgc 480 tccactccct acgtatgcct gcaggagcag gtcagactgc agtggcaagg ccaggaccct 540 gctcgctctg tcaccttcaa cagccagaag tttgagccca ccggcgtcgg ccacctggag 600 accctccaca tggccatgtc ctggcaggac cacggccgga tcctgcgctg ccagctctcc 660 gtggccaatc acagggctca gagcgagatt cacctccaag tgaagtatgc ccccaagggt 720 gtgaagatcc tcctcagccc ctcggggagg aacatccttc caggtgagct ggtcacactc 780 acctgccagg tgaacagcag ctaccctgca gtcagttcca ttaagtggct caaggatggg 840 gtacgcctcc aaaccaagac tggtgtgctg cacctgcccc aggcagcctg gagcgatgct 900 ggcgtctaca cctgccaagc tgagaacggc gtgggctctt tggtctcacc ccccatcagc 960 ctccacatct tcatggctga ggtccaggtg agcccagcag gtcccatcct ggagaaccag 1020 acagtgacac tagtctgcaa cacacccaat gaggcaccca gtgatctccg ctacagctgg 1080 tacaagaacc atgtcctgct ggaggatgcc cactcccata ccctccggct gcacttggcc 1140 actagggctg atactggctt ctacttctgt gaggtgcaga acgtccatgg cagcgagcgc 1200 tcgggccctg tcagcgtggt agtcaacctc ctgacagcct tcctggagac ccaggcggga 1260 cttgtgggca tccttcactg ctctgtggtc agtgagcccc tggccacact ggtgctgtca 1320 catgggggtc atatcctggc ctccacctcc ggggacagtg atcacagccc acgcttcagt 1380 ggtacctctg gtcccaactc cctgcgcctg gagatccgag acctggagga aactgacagt 1440 ggggagtaca agtgctcagc caccaactcc cttggaaatg caacctccac cctggacttc 1500 catgccaatg ccgcccgtct cctcatcagc ccggcagccg aggtggtgga aggacaggca 1560 gtgacactga gctgcagaag cggcctaagc cccacacctg atgcccgctt ctcctggtac 1620 ctgaatggag ccctgcttca cgagggtccc ggcagcagcc tcctgctccc cgcggcctcc 1680 agcactgacg ccggctcata ccactgccgg gcccgggacg gccacagtgc cagtggcccc 1740 tcttcgccag ctgttctcac tgtgctctac ccccctcgac aaccaacatt caccaccagg 1800 ctggaccttg atgccgctgg ggccggggct ggacggcgag gcctcctttt gtgccgtgtg 1860 gacagcgacc cccccgccag gctgcagctg ctccacaagg accgtgttgt ggccacttcc 1920 ctgccatcag ggggtggctg cagcacctgt gggggctgtt ccccacgcat gaaggtcacc 1980 aaagccccca acttgctgcg tgtggagatt cacaaccctt tgctggaaga ggagggcttg 2040 tacctctgtg aggccagcaa tgccctgggc aacgcctcca cctcagccac cttcaatggc 2100 caggccactg tcctggccat tgcaccatca cacacacttc aggagggcac agaagccaac 2160 ttgacttgca acgtgagccg ggaagctgct ggcagccctg ctaacttctc ctggttccga 2220 aatggggtgc tgtgggccca gggtcccctg gagaccgtga cactgctgcc cgtggccaga 2280 actgatgctg ccctttacgc ctgccgcatc ctgactgagg ctggtgccca gctctccact 2340 cccgtgctcc tgagtgtact ctatcccccg gaccgtccaa agctgtcagc cctcctagac 2400 atgggccagg gccacatggc tctgttcatc tgcactgtgg acagccgccc cctggccttg 2460 ctggccttgt tccatgggga gcacctcctg gccaccagcc tgggtcccca ggtcccatcc 2520 catggtcggt tccaggctaa agctgaggcc aactccctga agttagaggt ccgagaactg 2580 ggccttgggg actctggcag ctaccgctgt gaggccacaa atgttcttgg atcatccaac 2640 acctcactct tcttccaggt ccgaggagcc tgggtccagg tgtcaccatc acctgagctc 2700 caagagggcc aggctgtggt cctgagctgc caggtacaca caggagtccc agaggggacc 2760 tcatatcgtt ggtatcggga tggccagccc ctccaggagt cgacctcggc cacgctccgc 2820 tttgcagcca taactttgac acaagctggg gcctatcatt gccaagccca ggccccaggc 2880 tcagccacca cgagcctagc tgcacccatc agcctccacg tgtcctatgc cccacgccac 2940 gtcacactca ctaccctgat ggacacaggc cctggacgac tgggcctcct cctgtgccgt 3000 gtggacagtg accctccggc ccagctgcgg ctgctccacg gggatcgcct tgtggcctcc 3060 accctacaag gtgtgggggg acccgaaggc agctctccca ggctgcatgt ggctgtggcc 3120 cccaacacac tgcgtctgga gatccacggg gctatgctgg aggatgaggg tgtctatatc 3180 tgtgaggcct ccaacaccct gggccaggcc tcggcctcag ctgacttcga cgctcaagct 3240 gtgaatgtgc aggtgtggcc cggggctacc gtgcgggagg ggcagctggt gaacctgacc 3300 tgccttgtgt ggaccactca cccggcccag ctcacctaca catggtacca ggatgggcag 3360 cagcgcctgg atgcccactc catccccctg cccaacgtca cagtcaggga tgccacctcc 3420 taccgctgcg gtgtgggccc ccctggtcgg gcaccccgcc tctccagacc tatcaccttg 3480 gacgtcctct acgcgccccg caacctgcgc ctgacctacc tcctggagag ccatggcggg 3540 cagctggccc tggtactgtg cactgtggac agccgcccgc ccgcccagct ggccctcagc 3600 cacgccggtc gcctcttggc ctcctcgaca gcagcctctg tccccaacac cctgcgcctg 3660 gagctgcgag ggccacagcc cagggatgag ggtttctaca gctgctctgc ccgcagccct 3720 ctgggccagg ccaacacgtc cctggagctg cggctggagg gtgtgcgggt gatcctggct 3780 ccggaggctg ccgtgcctga aggtgccccc atcacagtga cctgtgcgga ccctgctgcc 3840 cacgcaccca cactctatac ttggtaccac aacggtcgtt ggctgcagga gggtccagct 3900 gcctcactct cattcctggt ggccacgcgg gctcatgcag gcgcctactc ttgccaggcc 3960 caggatgccc agggcacccg cagctcccgt cctgctgccc tgcaagtcct ctatgcccct 4020 caggacgctg tcctgtcctc cttccgggac tccagggcca gatccatggc tgtgatacag 4080 tgcactgtgg acagtgagcc acctgctgag ctggccctat ctcatgatgg caaggtgctg 4140 gccacgagca gcggggtcca cagcttggca tcagggacag gccatgtcca ggtggcccga 4200 aacgccctac ggctgcaggt gcaagatgtg cctgcaggtg atgacaccta tgtttgcaca 4260 gcccaaaact tgctgggctc aatcagcacc atcgggcggt tgcaggtaga aggtgcacgc 4320 gtggtggcag agcctggcct ggacgtgcct gagggcgctg ccctgaacct cagctgccgc 4380 ctcctgggtg gccctgggcc tgtgggcaac tccacctttg catggttctg gaatgaccgg 4440 cggctgcacg cggagcctgt gcccactctc gccttcaccc acgtggctcg tgctcaagct 4500 gggatgtacc actgcctggc tgagctcccc actggggctg ctgcctctgc tccagtcatg 4560 ctccgtgtgc tctaccctcc caagacgccc accatgatgg tcttcgtgga gcctgagggt 4620 ggcctccggg gcatcctgga ttgccgagtg gacagcgagc cgctcgccag cctgactctc 4680 caccttggca gtcgactggt ggcctccagt cagccccagg gtgctcctgc agagccacac 4740 atccatgtcc tggcttcccc caatgccctg agggtggaca tcgaggcgct gaggcccagc 4800 gaccaagggg aatacatctg ttctgcctca aatgtcctgg gctctgcctc tacctccacc 4860 tactttgggg tcagagccct gcaccgcctg catcagttcc agcagctgct ctgggtcctg 4920 ggactgctgg tgggcctcct gctcctgctg ttgggcctgg gggcctgcta cacctggaga 4980 aggaggcgtg tttgtaagca gagcatgggc gagaattcgg tggagatggc ttttcagaaa 5040 gagaccacgc agggactggg tactacctta ctggccctta caagagtgga gggcagacac 5100 agatgttgtc agcatcctta ttcctgctcc agatgcatct ctgttcatga ctgtgtga 5158 14 2238 DNA Homo sapiens 14 atgttccccc ttcgggccct gtggttggtc tgggcgcttc taggagtggc cggatcatgc 60 ccggagccgt gcgcctgcgt ggacaagtac gctcaccagt tcgcggactg cgcttacaaa 120 gagttgcgtg aggtgccgga aggactgcct gccaacgtga cgacgcttag tctgtccgcg 180 aacaagatca ctgtgctgcg gcgcggggcc ttcgccgacg tcacacaggt cacgtcgctg 240 tggctggcgc acaatgaggt gcgcaccgtg gagccaggcg cactggccgt gctgagtcag 300 ctcaagaacc tcgatctgag ccacaacttc atatccagct ttccgtggag cgacctgcgc 360 aacctgagcg cgctgcagct gctcaaaatg aaccacaacc gcctgggctc tctgccccgg 420 gacgcactcg gtgcgctacc cgacctgcgt tccctgcgca tcaacaacaa ccggctgcgt 480 acgctggcgc ctggcacctt cgacgcgctt agcgcgctgt cacacttgca actctatcac 540 aatcccttcc actgcggctg cggccttgtg tggctgcagg cctgggccgc gagcacccgg 600 gtgtccttac ccgagcccga ctccattgct tgtgcctcgc ctcccgcgct gcagggggtg 660 ccggtgtacc gcctgcccgc cctgccctgt gcaccgccca gcgtgcatct gagtgccgag 720 ccaccgcttg aagcacccgg caccccactg cgcgcaggac tggcgttcgt gttacactgc 780 atcgccgacg gccaccctac gcctcgcctg caatggcaac ttcagatccc cggtggcacc 840 gtagtcttag agccaccggt tctgagcggg gaggacgacg gggttggggc ggaggaagga 900 gagggagaag gagatgggga tttgctgacg cagacccaag cccaaacgcc gactccagca 960 cccgcttggc cggcgccccc agccacaccg cgcttcctgg ccctcgcaaa tggctccctg 1020 ttggtgcccc tcctgagtgc caaggaggcg ggcgtctaca cttgccgtgc acacaatgag 1080 ctgggcgcca actctacgtc aatacgcgtg gcggtggcag caaccgggcc cccaaaacac 1140 gcgcctggcg ccgggggaga acccgacgga caggccccga cctctgagcg caagtccaca 1200 gccaagggcc ggggcaacag cgtcctgcct tccaaacccg agggcaaaat caaaggccaa 1260 ggcctggcca aggtcagcat tctcggggag accgagacgg agccggagga ggacacaagt 1320 gagggagagg aggccgaaga ccagatcctc gcggacccgg cggaggagca gcgctgtggc 1380 aacggggacc cctctcggta cgtttctaac cacgcgttca accagagcgc agagctcaag 1440 ccgcacgtct tcgagctggg cgtcatcgcg ctggatgtgg cggagcgcga ggcgcgggtg 1500 cagctgactc cgctggctgc gcgctggggc cctgggcccg gcggggctgg cggagccccg 1560 cgacccgggc ggcgacccct gcgcctactc tatctgtgtc cagcgggggg cggcgcggca 1620 gtgcagtggt cccgcgtaga ggaaggcgtc aacgcctact ggttccgcgg cctgcggccg 1680 ggtaccaact actccgtgtg cctggcgctg gcgggcgaag cctgccacgt gcaagtggtg 1740 ttttccacca agaaggagct cccatcgctg ctggtcatag tggcagtgag cgtattcctc 1800 ctggtgctgg ccacagtgcc ccttctgggc gccgcctgct gccatctgct ggctaaacac 1860 ccgggcaagc cctaccgtct gatcctgcgg cctcaggccc ctgaccctat ggagaagcgc 1920 atcgccgcag acttcgaccc gcgtgcttcg tacctcgagt ccgagaaaag ctacccggca 1980 ggcggcgagg cgggcggcga ggagccagag gacgtgcagg gggagggcct tgatgaagac 2040 gcggagcagg gagacccaag tggggacctg cagagagagg agagcctggc ggcctgctca 2100 ctggtggagt cccagtccaa ggccaaccaa gaggagttcg aggcgggctc tgagtacagc 2160 gatcggctgc ccctgggcgc cgaggcggtc aacatcgccc aggagattaa tggcaactac 2220 aggcagacgg caggctga 2238 15 756 DNA Homo sapiens 15 atgtcggcct acggcatgcc catgtacaag agcggggacc tggtgtttgc caagttaaag 60 ggctatgccc actggccggc gaggatagag cacatgaccc agcccaaccg ctaccaggtg 120 tttttcttcg ggacccacga gacggccttc ctgagtccca aacgcctgtt cccgtacaag 180 gagtgcaagg agaagttcgg caagcccaac aagaggcgcg gcttcagcgc ggggctgtgg 240 gaaatcgaga acaaccccac ggtccaggcc tccgactgcc cattagcctc agagaagggc 300 agcggagacg ggccttggcc ggagcccgag gccgcagagg gcgacgagga caagccgacc 360 cacgctggtg gcggcggcga cgaattgggg aagccggacg acgacaagcc cactgaggag 420 gagaaggggc cgctgaagag gagcgcgggg gacccgccgg aggacgcccc caaacgaccc 480 aaggaggcag cccccgacca agaggaggag gcggaggcgg agagggcggc ggaagcggag 540 agggcggcgg cggcggcggc ggcgacggcc gtcgacgagg agagtccgtt cctcgtggcg 600 gtggagaacg gcagcgcccc tagcgagccg ggcctggtct gcgagccgcc tcagccagag 660 gaggaggagc tccgggagga agaagtcgcg gacgaggagg cctcccagga gtggcatgcc 720 gaggcaccgg gcggcggaga tcgcgacagc ctgtag 756 16 1224 DNA Homo sapiens 16 tttctaataa gtgaccgtga cccacagtgc aacctccact gctccaggac tcaacccaaa 60 cccatctgtg cctctgatgg caggtcctac gagtccatgt gtgagtacca gcgagccaag 120 tgccgagacc cgaccctggg cgtggtgcat cgaggtagat gcaaagatgc tggccagagc 180 aagtgtcgcc tggagcgggc tcaagccctg gagcaagcca agaagcctca ggaagctgtg 240 tttgtcccag agtgtggcga ggatggctcc tttacccagg tgcagtgcca tacttacact 300 gggtactgct ggtgtgtcac cccggatggg aagcccatca gtggctcttc tgtgcagaat 360 aaaactcctg tatgttcagg ttcagtcacc gacaagccct tgagccaggg taactcagga 420 aggaaagatg acgggtctaa gccgacaccc acgatggaga cccagccggt gttcgatgga 480 gatgaaatca cagccccaac tctatggatt aaacacttgg tgatcaagga ctccaaactg 540 aacaacacca acataagaaa ttcagagaaa gtctattcgt gtgaccagga gaggcagagt 600 gccctggaag aggcccagca gaatccccgt gagggtattg tcatccctga atgtgcccct 660 gggggactct ataagccagt gcaatgccac cagtccactg gctactgctg gtgtgtgctg 720 gtggacacag ggcgcccgct gcctgggacc tccacacgct acgtgatgcc cagttgtgag 780 agcgacgcca gggccaagac tacagaggcg gatgacccct tcaaggacag ggagctacca 840 ggctgtccag aagggaagaa aatggagttt atcaccagcc tactggatgc tctcaccact 900 gacatggttc aggccattaa ctcagcagcg cccactggag gtgggaggtt ctcagagcca 960 gaccccagcc acaccctgga ggagcgggta gtgcactggt atttcagcca gctggacagc 1020 aatagcagca acgacattaa caagcgggag atgaagccct tcaagcgcta cgtgaagaag 1080 aaagccaagc ccaagaaatg tgcccggcgt ttcaccgact actgtgacct gaacaaagac 1140 aaggtcattt cactgcctga gctgaagggc tgcctgggtg ttagcaaaga aggtggtagc 1200 cttggcagtt tcccccaggc aaaa 1224 17 1305 DNA Homo sapiens 17 atggcaggct ctgggccacc tctgcccacg tgcaatgcag aagtgggatg ggagaacatg 60 gctgaggacg gcaaggcttt tctaataagt gaccgtgacc cacagtgcaa cctccactgc 120 tccaggactc aacccaaacc catctgtgcc tctgatggca ggtcctacga gtccatgtgt 180 gagtaccagc gagccaagtg ccgagacccg accctgggcg tggtgcatcg aggtagatgc 240 aaagatgctg gccagagcaa gtgtcgcctg gagcgggctc aagccctgga gcaagccaag 300 aagcctcagg aagctgtgtt tgtcccagag tgtggcgagg atggctcctt tacccaggtg 360 cagtgccata cttacactgg gtactgctgg tgtgtcaccc cggatgggaa gcccatcagt 420 ggctcttctg tgcagaataa aactcctgta tgttcaggtt cagtcaccga caagcccttg 480 agccagggta actcaggaag gaaagatgac gggtctaagc cgacacccac gatggagacc 540 cagccggtgt tcgatggaga tgaaatcaca gccccaactc tatggattaa acacttggtg 600 atcaaggact ccaaactgaa caacaccaac ataagaaatt cagagaaagt ctattcgtgt 660 gaccaggaga ggcagagtgc cctggaagag gcccagcaga atccccgtga gggtattgtc 720 atccctgaat gtgcccctgg gggactctat aagccagtgc aatgccacca gtccactggc 780 tactgctggt gtgtgctggt ggacacaggg cgcccgctgc ctgggacctc cacacgctac 840 gtgatgccca gttgtgagag cgacgccagg gccaagacta cagaggcgga tgaccccttc 900 aaggacaggg agctaccagg ctgtccagaa gggaagaaaa tggagtttat caccagccta 960 ctggatgctc tcaccactga catggttcag gccattaact cagcagcgcc cactggaggt 1020 gggaggttct cagagccaga ccccagccac accctggagg agcgggtagt gcactggtat 1080 ttcagccagc tggacagcaa tagcagcaac gacattaaca agcgggagat gaagcccttc 1140 aagcgctacg tgaagaagaa agccaagccc aagaaatgtg cccggcgttt caccgactac 1200 tgtgacctga acaaagacaa ggtcatttca ctgcctgagc tgaagggctg cctgggtgtt 1260 agcaaagaag gtggtagcct tggcagtttc ccccaggcaa aatga 1305 18 753 DNA Homo sapiens 18 atggcatgct ggtggccgct cctgctagag ctgtggacag tcatgcccac ctgggctggg 60 gacgagctgc tcaacatctg catgaatgcc aaacaccaca agagagtgcc cagcccagaa 120 gacaagctct atgaggagtg catcccctgg aaggacaatg cctgctgcac cctcacgaca 180 agctgggaag cccatctgga tgtatcccca ctctacaact tcagcctgtt tcactgtgga 240 ctgctgatgc ctggctgtcg gaagcacttc atccaggcta tctgcttcta tgagtgctcc 300 ccaaacctgg ggccctggat ccagccagtg ggaagcctgg ggtgggaggt ggccccgagt 360 gggcagggag agcgagttgt gaatgtgccg ctgtgccagg aggactgtga ggagtggtgg 420 gaagactgtc gcatgtctta cacatgcaaa tccaactggc gtggtggctg ggactggagt 480 caggggaaga accgctgccc caaaggggcc cagtgcctcc ctttctccca ttacttcccc 540 accccagctg acctgtgtga gaagacttgg agcaattcct tcaaagccag ccctgagcga 600 cggaacagtg ggcggtgtct ccagaagtgg tttgagcctg ctcagggcaa ccccaatgtg 660 gccgtggccc gcctcttcgc cagctctgcc ccatcctggg aactgtccta caccatcatg 720 gtctgctccc tgttcctgcc gttcctttcc tga 753 19 774 DNA Homo sapiens 19 atgggcaccg tgcgcccacc tcgcccctcg ctcctgctgg tctccacccg ggagtcttgt 60 ctcttcctcc tcttctgcct gcacctgggc gccgcctgcc cacagccctg ccggtgccct 120 gaccacgcag gggctgtggc tgtcttctgc agcttgcggg gccttcagga ggtccccgag 180 gacatcccgg ccaacaccgt gctcctgaag ctcgatgcca acaagatctc ccacctcccg 240 gacggggcct tccagcacct gcaccggctc agggagctgg atctgtctca caacgccatc 300 gaggccatcg gctccgccac cttcgcgggc ctggccgggg gcctgcggct gctggacctg 360 tcttacaacc gcatccagag gatccccaag gacgccctgg gcaaactcag cgccaagata 420 cgcctgtccc acaaccccct gcactgcgag tgcgccctgc aggaggccct gtgggagctg 480 aagctggacc ccgactctgt ggacgagatc gcctgccaca cctcagtgca ggaggagttt 540 gtggggaagc ctctggttca ggctctggat gcgggtgcca gcctctgcag cgtcccccac 600 aggaccacag acgtggccat gctggtcacc atgttcggct ggttcgccat ggtgatcgcc 660 tacgtcgtgt actatgtgcg ccacaaccag gaggatgccc ggaggcacct ggagtacctg 720 aagtctctgc ccagcgcccc cgcctccaag gaccccatcg gcccggggcc ctag 774 20 447 DNA Homo sapiens 20 atgctgggcc tgccgtggaa gggaggtctg tcctgggcgc tgctgctgct tctcttaggc 60 tcccagatcc tgctgatcta tgcctggcat ttccacgagc aaagggactg tgatgaacac 120 aatgtcatgg ctcgttacct ccctgccaca gtggagtttg ctgtccacac attcaaccaa 180 cagagcaagg actactatgc ctacagactg gggcacatct tgaattcctg gaaggagcag 240 gtggagtcca agactgtatt ctcaatggag ctactgctgg ggagaactag gtgtgggaaa 300 tttgaagacg acattgacaa ctgccatttc caagaaagca cagagctgaa caatgtaaga 360 caggacacca gcttccctcc tggatacagc tgtggatgcc acatggggtg tggtgtgggc 420 acaggtgcaa ctgacaaaga gacttag 447 21 1068 DNA Homo sapiens 21 atgggaccta aagacagtgc caagtgcctg caccgtggac cacagccgag ccactgggca 60 gccggtgatg gtcccacgca ggagcgctgt ggaccccgct ctctgggcag ccctgtccta 120 ggcctggaca cctgcagagc ctgggaccac gtggatgggc agatcctggg ccagctgcgg 180 cccctgacag aggaggaaga ggaggagggc gccggggcca ccttgtccag ggggcctgcc 240 ttccccggca tgggctctga ggagttgcgt ctggcctcct tctatgactg gccgctgact 300 gctgaggtgc cacccgagct gctggctgct gccggcttct tccacacagg ccatcaggac 360 aaggtgaggt gcttcttctg ctatgggggc ctgcagagct ggaagcgcgg ggacgacccc 420 tggacggagc atgccaagtg gttccccagc tgtcagttcc tgctccggtc aaaaggaaga 480 gactttgtcc acagtgtgca ggagactcac tcccagctgc tgggctcctg ggtgagcgcc 540 acctctcctc ggggctccgg gtggcagtgg ggtcctgccc ctcctatttc cccaaggcct 600 gatggtctct ggctccttcc aggacccgtg ggaagaaccg gaagacgcag cccctgtggc 660 cccctccggt ccagtctgaa agtgcccagg agccaggtgc aggcccggga ccccctgggt 720 gagggctggg gcaggggagg gctgagggac cccgaccttc catggcccat agagggtggg 780 ggccagggtg tggggacatt tcgcaggcct gtcctcctag gaggggtcag tccagccgag 840 gcccagaggg cgtggtgggt tcttgagccc ccaggagcca gggatgtgga ggcgcagctg 900 cggcggctgc aggaggagag gacgtgcaag gtgtgcctgg accgcgccgt gtccatcgtc 960 tttgtgccgt gcggccacct ggtctgtgct gagtgtgccc ccggcctgca gctgtgcccc 1020 atctgcagag cccccgtccg cagccgcgtg cgcaccttcc tgtcctag 1068 22 769 DNA Homo sapiens 22 atgggaccta aagacagtgc caagtgcctg caccgtggac cacagccgag ccactgggca 60 gccggtgatg gtcccacgca ggagcgctgt ggaccccgct ctctgggcag ccctgtccta 120 ggcctggaca cctgcagagc ctgggaccac gtggatgggc agatcctggg ccagctgcgg 180 cccctgacag aggaggaaga ggaggagggc gccggggcca ccttgtccag ggggcctgcc 240 ttccccggca tgggctctga ggagttgcgt ctggcctcct tctatgactg gccgctgact 300 gctgaggtgc cacccgagct gctggctgct gccggcttct tccacacagg ccatcaggac 360 aaggtgaggt gcttcttctg ctatgggggc ctgcagagct ggaagcgcgg ggacgacccc 420 tggacggagc atgccaagtg gttccccctg tcagttcctg ctccggtcaa aaggaagaga 480 ctttgtccac agtgtgcagg agactcactc ccagctgctg ggctcctggg acccgtggga 540 agaaccggaa gacgcagccc ctgtggcccc ctccggagcc agggatgtgg aggcgcagct 600 gcggcggctg caggaggaga ggacgtgcaa ggtgtgcctg gaccgcgccg tgtccatcgt 660 ctttgtgccg tgcggccacc tggtctgtgc tgagtgtgcc cccggcctgc agctgtgccc 720 catctgcaga gcccccgtcc gcagccgcgt gcgcaccttc ctgtcctag 769 23 756 DNA Homo sapiens 23 atgttggggg cccgcctcag gctctgggtc tgtgccttgt gcagcgtctg cagcatgagc 60 gtcctcagag cctatcccaa tgcctcccca ctgctcggct ccagctgggg tggcctgatc 120 cacctgtaca cagccacagc caggaacagc taccacctgc agatccacaa gaatggccat 180 gtggatggcg caccccatca gaccatctac agtgccctga tgatcagatc agaggatgct 240 ggctttgtgg tgattacagg tgtgatgagc agaagatacc tctgcatgga tttcagaggc 300 aacatttttg gatcacacta tttcgacccg gagaactgca ggttccaaca ccagacgctg 360 gaaaacgggt acgacgtcta ccactctcct cagtatcact tcctggtcag tctgggccgg 420 gcgaagagag ccttcctgcc aggcatgaac ccacccccgt actcccagtt cctgtcccgg 480 aggaacgaga tccccctaat tcacttcaac acccccatac cacggcggca cacccggagc 540 gccgaggacg actcggagcg ggaccccctg aacgtgctga agccccgggc ccggatgacc 600 ccggccccgg cctcctgttc acaggagctc ccgagcgccg aggacaacag cccgatggcc 660 agtgacccat taggggtggt caggggcggt cgagtgaaca cgcacgctgg gggaacgggc 720 ccggaaggct gccgcccctt cgccaagttc atctag 756 24 592 PRT Homo sapiens 24 Met Thr Cys Trp Leu Cys Val Leu Ser Leu Pro Leu Leu Leu Leu Pro 1 5 10 15 Ala Ala Pro Pro Pro Ala Gly Gly Cys Pro Ala Arg Cys Glu Cys Thr 20 25 30 Val Gln Thr Arg Ala Val Ala Cys Thr Arg Arg Arg Leu Thr Ala Val 35 40 45 Pro Asp Gly Ile Pro Ala Glu Thr Arg Leu Leu Glu Leu Ser Arg Asn 50 55 60 Arg Ile Arg Cys Leu Asn Pro Gly Asp Leu Ala Ala Leu Pro Ala Leu 65 70 75 80 Glu Glu Leu Asp Leu Ser Glu Asn Ala Ile Ala His Val Glu Pro Gly 85 90 95 Ala Phe Ala Asn Leu Pro Arg Leu Arg Val Leu Arg Leu Arg Gly Asn 100 105 110 Gln Leu Lys Leu Ile Pro Pro Gly Val Phe Thr Arg Leu Asp Asn Leu 115 120 125 Thr Leu Leu Asp Leu Ser Glu Asn Lys Leu Val Ile Leu Leu Asp Tyr 130 135 140 Thr Phe Gln Asp Leu His Ser Leu Arg Arg Leu Glu Val Gly Asp Asn 145 150 155 160 Asp Leu Val Phe Val Ser Arg Arg Ala Phe Ala Gly Leu Leu Ala Leu 165 170 175 Glu Glu Leu Thr Leu Glu Arg Cys Asn Leu Thr Ala Leu Ser Gly Glu 180 185 190 Ser Leu Gly His Leu Arg Ser Leu Gly Ala Leu Arg Leu Arg His Leu 195 200 205 Ala Ile Ala Ser Leu Glu Asp Gln Asn Phe Arg Arg Leu Pro Gly Leu 210 215 220 Leu His Leu Glu Ile Asp Asn Trp Pro Leu Leu Glu Glu Val Ala Ala 225 230 235 240 Gly Ser Leu Arg Gly Leu Asn Leu Thr Ser Leu Ser Val Thr His Thr 245 250 255 Asn Ile Thr Ala Val Pro Ala Ala Ala Leu Arg His Gln Ala His Leu 260 265 270 Thr Cys Leu Asn Leu Ser His Asn Pro Ile Ser Thr Val Pro Arg Gly 275 280 285 Ser Phe Arg Asp Leu Val Arg Leu Arg Glu Leu His Leu Ala Gly Ala 290 295 300 Leu Leu Ala Val Val Glu Pro Gln Ala Phe Leu Gly Leu Arg Gln Ile 305 310 315 320 Arg Leu Leu Asn Leu Ser Asn Asn Leu Leu Ser Thr Leu Glu Glu Ser 325 330 335 Thr Phe His Ser Val Asn Thr Leu Glu Thr Leu Arg Val Asp Gly Asn 340 345 350 Pro Leu Ala Cys Asp Cys Arg Leu Leu Trp Ile Val Gln Arg Arg Lys 355 360 365 Thr Leu Asn Phe Asp Gly Arg Leu Pro Ala Cys Ala Thr Pro Ala Glu 370 375 380 Val Arg Gly Asp Ala Leu Arg Asn Leu Pro Asp Ser Val Leu Phe Glu 385 390 395 400 Tyr Phe Val Cys Arg Lys Pro Lys Ile Arg Glu Arg Arg Leu Gln Arg 405 410 415 Val Thr Ala Thr Ala Gly Glu Asp Val Arg Phe Leu Cys Arg Ala Glu 420 425 430 Gly Glu Pro Ala Pro Thr Val Ala Trp Val Thr Pro Gln His Arg Pro 435 440 445 Val Thr Ala Thr Ser Ala Gly Arg Ala Arg Val Leu Pro Gly Gly Thr 450 455 460 Leu Glu Ile Gln Asp Ala Arg Pro Gln Asp Ser Gly Thr Tyr Thr Cys 465 470 475 480 Val Ala Ser Asn Ala Gly Gly Asn Asp Thr Tyr Phe Ala Thr Leu Thr 485 490 495 Val Arg Pro Glu Pro Ala Ala Asn Arg Thr Pro Gly Glu Ala His Asn 500 505 510 Glu Thr Leu Ala Ala Leu Arg Ala Pro Leu Asp Leu Thr Thr Ile Leu 515 520 525 Val Ser Thr Ala Met Gly Cys Ile Thr Phe Leu Gly Val Val Leu Phe 530 535 540 Cys Phe Val Leu Leu Phe Val Trp Ser Arg Gly Arg Gly Gln His Lys 545 550 555 560 Asn Asn Phe Ser Val Glu Tyr Ser Phe Arg Lys Val Asp Gly Pro Ala 565 570 575 Ala Ala Ala Gly Gln Gly Gly Ala Arg Lys Phe Asn Met Lys Met Ile 580 585 590 25 653 PRT Homo sapiens 25 Met Lys Leu Leu Trp Gln Val Thr Val His His His Thr Trp Asn Ala 1 5 10 15 Ile Leu Leu Pro Phe Val Tyr Leu Thr Ala Gln Val Trp Ile Leu Cys 20 25 30 Ala Ala Ile Ala Ala Ala Ala Ser Ala Gly Pro Gln Asn Cys Pro Ser 35 40 45 Val Cys Ser Cys Ser Asn Gln Phe Ser Lys Val Val Cys Thr Arg Arg 50 55 60 Gly Leu Ser Glu Val Pro Gln Gly Ile Pro Ser Asn Thr Arg Tyr Leu 65 70 75 80 Asn Leu Met Glu Asn Asn Ile Gln Met Ile Gln Ala Asp Thr Phe Arg 85 90 95 His Leu His His Leu Glu Val Leu Gln Leu Gly Arg Asn Ser Ile Arg 100 105 110 Gln Ile Glu Val Gly Ala Phe Asn Gly Leu Ala Ser Leu Asn Thr Leu 115 120 125 Glu Leu Phe Asp Asn Trp Leu Thr Val Ile Pro Ser Gly Ala Phe Glu 130 135 140 Tyr Leu Ser Lys Leu Arg Glu Leu Trp Leu Arg Asn Asn Pro Ile Glu 145 150 155 160 Ser Ile Pro Ser Tyr Ala Phe Asn Arg Val Pro Ser Leu Met Arg Leu 165 170 175 Asp Leu Gly Glu Leu Lys Lys Leu Glu Tyr Ile Ser Glu Gly Ala Phe 180 185 190 Glu Gly Leu Phe Asn Leu Lys Tyr Leu Asn Leu Gly Met Cys Asn Ile 195 200 205 Lys Asp Met Pro Asn Leu Thr Pro Leu Val Gly Leu Glu Glu Leu Glu 210 215 220 Met Ser Gly Asn His Phe Pro Glu Ile Arg Pro Gly Ser Phe His Gly 225 230 235 240 Leu Ser Ser Leu Lys Lys Leu Trp Val Met Asn Ser Gln Val Ser Leu 245 250 255 Ile Glu Arg Asn Ala Phe Asp Gly Leu Ala Ser Leu Val Glu Leu Asn 260 265 270 Leu Ala His Asn Asn Leu Ser Ser Leu Pro His Asp Leu Phe Thr Pro 275 280 285 Leu Arg Tyr Leu Val Glu Leu His Leu His His Asn Pro Trp Asn Cys 290 295 300 Asp Cys Asp Ile Leu Trp Leu Ala Trp Trp Leu Arg Glu Tyr Ile Pro 305 310 315 320 Thr Asn Ser Thr Cys Cys Gly Arg Cys His Ala Pro Met His Met Arg 325 330 335 Gly Arg Tyr Leu Val Glu Val Asp Gln Ala Ser Phe Gln Cys Ser Ala 340 345 350 Pro Phe Ile Met Asp Ala Pro Arg Asp Leu Asn Ile Ser Glu Gly Arg 355 360 365 Met Ala Glu Leu Lys Cys Arg Thr Pro Pro Met Ser Ser Val Lys Trp 370 375 380 Leu Leu Pro Asn Gly Thr Val Leu Ser His Ala Ser Arg His Pro Arg 385 390 395 400 Ile Ser Val Leu Asn Asp Gly Thr Leu Asn Phe Ser His Val Leu Leu 405 410 415 Ser Asp Thr Gly Val Tyr Thr Cys Met Val Thr Asn Val Ala Gly Asn 420 425 430 Ser Asn Ala Ser Ala Tyr Leu Asn Val Ser Thr Ala Glu Leu Asn Thr 435 440 445 Ser Asn Tyr Ser Phe Phe Thr Thr Val Thr Val Glu Thr Thr Glu Ile 450 455 460 Ser Pro Glu Asp Thr Thr Arg Lys Tyr Lys Pro Val Pro Thr Thr Ser 465 470 475 480 Thr Gly Tyr Gln Pro Ala Tyr Thr Thr Ser Thr Thr Val Leu Ile Gln 485 490 495 Thr Thr Arg Val Pro Lys Gln Val Ala Val Pro Ala Thr Asp Thr Thr 500 505 510 Asp Lys Met Gln Thr Ser Leu Asp Glu Val Met Lys Thr Thr Lys Ile 515 520 525 Ile Ile Gly Cys Phe Val Ala Val Thr Leu Leu Ala Ala Ala Met Leu 530 535 540 Ile Val Phe Tyr Lys Leu Arg Lys Arg His Gln Gln Arg Ser Thr Val 545 550 555 560 Thr Ala Ala Arg Thr Val Glu Ile Ile Gln Val Asp Glu Asp Ile Pro 565 570 575 Ala Ala Thr Ser Ala Ala Ala Thr Ala Ala Pro Ser Gly Val Ser Gly 580 585 590 Glu Gly Ala Val Val Leu Pro Thr Ile His Asp His Ile Asn Tyr Asn 595 600 605 Thr Tyr Lys Pro Ala His Gly Ala His Trp Thr Glu Asn Ser Leu Gly 610 615 620 Asn Ser Leu His Pro Thr Val Thr Thr Ile Ser Glu Pro Tyr Ile Ile 625 630 635 640 Gln Thr His Thr Lys Asp Lys Val Gln Glu Thr Gln Ile 645 650 26 70 PRT Homo sapiens 26 Met Val Ser Val Cys Arg Pro Trp Pro Ala Val Ala Ile Ala Leu Leu 1 5 10 15 Ala Leu Leu Val Cys Leu Gly Ala Leu Val Asp Thr Cys Pro Ile Lys 20 25 30 Pro Glu Ala Pro Gly Glu Asp Glu Ser Leu Glu Glu Leu Ser His Tyr 35 40 45 Tyr Ala Ser Leu Cys His Tyr Leu Asn Val Val Thr Arg Gln Trp Trp 50 55 60 Glu Gly Ala Asp Met Trp 65 70 27 130 PRT Homo sapiens 27 Met Lys Leu Ala Phe Leu Phe Leu Gly Pro Met Ala Leu Leu Leu Leu 1 5 10 15 Ala Gly Tyr Gly Cys Val Leu Gly Ala Ser Ser Gly Asn Leu Arg Thr 20 25 30 Phe Val Gly Cys Ala Val Arg Glu Phe Thr Phe Leu Ala Lys Lys Pro 35 40 45 Gly Cys Arg Gly Leu Arg Ile Thr Thr Asp Ala Cys Trp Gly Arg Cys 50 55 60 Glu Thr Trp Glu Lys Pro Ile Leu Glu Pro Pro Tyr Ile Glu Ala His 65 70 75 80 His Arg Val Cys Thr Tyr Asn Glu Thr Lys Gln Val Thr Val Lys Leu 85 90 95 Pro Asn Cys Ala Pro Gly Val Asp Pro Phe Tyr Thr Tyr Pro Val Ala 100 105 110 Ile Arg Cys Asp Cys Gly Ala Cys Ser Thr Ala Thr Thr Glu Cys Glu 115 120 125 Thr Ile 130 28 676 PRT Homo sapiens 28 Ile Pro Asn Ala Phe Lys Pro Gly Asp Leu Val Phe Pro Lys Ile Lys 1 5 10 15 Gly Tyr Pro Gln Trp Pro Ser Arg Ile Asp Asp Ile Ala Asp Gly Ala 20 25 30 Val Lys Pro Pro Pro Asn Lys Tyr Pro Ile Phe Phe Phe Gly Thr His 35 40 45 Glu Thr Ala Phe Leu Gly Pro Lys Asp Leu Phe Pro Tyr Asp Lys Cys 50 55 60 Lys Asp Lys Tyr Gly Lys Pro Asn Lys Arg Lys Gly Phe Asn Glu Gly 65 70 75 80 Leu Trp Glu Ile Gln Asn Asn Pro His Ala Ser Tyr Ser Ala Pro Pro 85 90 95 Pro Val Ser Ser Ser Asp Ser Glu Ala Pro Glu Ala Asn Pro Ala Asp 100 105 110 Gly Ser Asp Ala Asp Glu Asp Asp Glu Asp Arg Gly Val Met Ala Val 115 120 125 Thr Ala Val Thr Ala Thr Ala Ala Ser Asp Arg Met Glu Ser Asp Ser 130 135 140 Asp Ser Asp Lys Ser Ser Asp Asn Ser Gly Leu Lys Arg Lys Thr Pro 145 150 155 160 Ala Leu Lys Met Ser Val Ser Lys Arg Ala Arg Lys Ala Ser Ser Asp 165 170 175 Leu Asp Gln Ala Ser Val Ser Pro Ser Glu Glu Glu Asn Ser Glu Ser 180 185 190 Ser Ser Glu Ser Glu Lys Thr Ser Asp Gln Asp Phe Thr Pro Glu Lys 195 200 205 Lys Ala Ala Val Arg Ala Pro Arg Arg Gly Pro Leu Gly Gly Arg Lys 210 215 220 Lys Lys Lys Ala Pro Ser Ala Ser Asp Ser Asp Ser Lys Ala Asp Ser 225 230 235 240 Asp Gly Ala Lys Pro Glu Pro Val Ala Met Ala Arg Ser Ala Ser Ser 245 250 255 Ser Ser Ser Ser Ser Ser Ser Ser Asp Ser Asp Val Ser Val Lys Lys 260 265 270 Pro Pro Arg Gly Arg Lys Pro Ala Glu Lys Pro Leu Pro Lys Pro Arg 275 280 285 Gly Arg Lys Pro Lys Pro Glu Arg Pro Pro Ser Ser Ser Ser Ser Asp 290 295 300 Ser Asp Ser Asp Glu Val Asp Arg Ile Ser Glu Trp Lys Arg Arg Asp 305 310 315 320 Glu Ala Arg Arg Arg Glu Leu Glu Ala Arg Arg Arg Arg Glu Gln Glu 325 330 335 Glu Glu Leu Arg Arg Leu Arg Glu Gln Glu Lys Glu Glu Lys Glu Arg 340 345 350 Arg Arg Glu Arg Ala Asp Arg Gly Glu Ala Glu Arg Gly Ser Gly Gly 355 360 365 Ser Ser Gly Asp Glu Leu Arg Glu Asp Asp Glu Pro Val Lys Lys Arg 370 375 380 Gly Arg Lys Gly Arg Gly Arg Gly Pro Pro Ser Ser Ser Asp Ser Glu 385 390 395 400 Pro Glu Ala Glu Leu Glu Arg Glu Ala Lys Lys Ser Ala Lys Lys Pro 405 410 415 Gln Ser Ser Ser Thr Glu Pro Ala Arg Lys Pro Gly Gln Lys Glu Lys 420 425 430 Arg Val Arg Pro Glu Glu Lys Gln Gln Ala Lys Pro Val Lys Val Glu 435 440 445 Arg Thr Arg Lys Arg Ser Glu Gly Phe Ser Met Asp Arg Lys Val Glu 450 455 460 Lys Lys Lys Glu Pro Ser Val Glu Glu Lys Leu Gln Lys Leu His Ser 465 470 475 480 Glu Ile Lys Phe Ala Leu Lys Val Asp Ser Pro Asp Val Lys Arg Cys 485 490 495 Leu Asn Ala Leu Glu Glu Leu Gly Thr Leu Gln Val Thr Ser Gln Ile 500 505 510 Leu Gln Lys Asn Thr Asp Val Val Ala Thr Leu Lys Lys Ile Arg Arg 515 520 525 Tyr Lys Ala Asn Lys Asp Val Met Glu Lys Ala Ala Glu Val Tyr Thr 530 535 540 Arg Leu Lys Ser Arg Val Leu Gly Pro Lys Ile Glu Ala Val Gln Lys 545 550 555 560 Val Asn Lys Ala Gly Met Glu Lys Glu Lys Ala Glu Glu Lys Leu Ala 565 570 575 Gly Glu Glu Leu Ala Gly Glu Glu Leu Ala Gly Glu Glu Ala Pro Gln 580 585 590 Glu Lys Ala Glu Asp Lys Pro Ser Thr Asp Leu Ser Ala Pro Val Asn 595 600 605 Gly Glu Ala Thr Ser Gln Lys Gly Glu Ser Ala Glu Asp Lys Glu His 610 615 620 Glu Glu Gly Arg Asp Ser Glu Glu Gly Pro Arg Cys Gly Ser Ser Glu 625 630 635 640 Asp Leu His Asp Ser Val Arg Glu Gly Pro Asp Leu Asp Arg Pro Gly 645 650 655 Ser Asp Arg Gln Glu Arg Glu Arg Ala Arg Gly Asp Ser Glu Ala Leu 660 665 670 Asp Glu Glu Ser 675 29 717 PRT Homo sapiens 29 Met Ala Val Leu Asp Leu Arg Glu Leu Arg Arg Gly Asp Leu Gly Gly 1 5 10 15 Val Gln Gly Leu Lys Glu Leu Arg Arg Gln Trp Ser Gly Gly Pro Gly 20 25 30 Pro Glu Glu Ala Ala Leu Trp Gly Ser Gly Ala Ser Val Pro Glu Gly 35 40 45 Ala Ala Pro Trp Gly Ser Gly Val Ala Leu Ala Gln Arg Glu Pro Arg 50 55 60 Leu Ile Asp Asp Ile Ala Asp Gly Ala Val Lys Pro Pro Pro Asn Lys 65 70 75 80 Tyr Pro Ile Phe Phe Phe Gly Thr His Glu Thr Ala Phe Leu Gly Pro 85 90 95 Lys Asp Leu Phe Pro Tyr Asp Lys Cys Lys Asp Lys Tyr Gly Lys Pro 100 105 110 Asn Lys Arg Lys Gly Phe Asn Glu Gly Leu Trp Glu Ile Gln Asn Asn 115 120 125 Pro His Ala Ser Tyr Ser Ala Pro Pro Pro Val Ser Ser Ser Asp Ser 130 135 140 Glu Ala Pro Glu Ala Asn Pro Ala Asp Gly Ser Asp Ala Asp Glu Asp 145 150 155 160 Asp Glu Asp Arg Gly Val Met Ala Val Thr Ala Val Thr Ala Thr Ala 165 170 175 Ala Ser Asp Arg Met Glu Ser Asp Ser Asp Ser Asp Lys Ser Ser Asp 180 185 190 Asn Ser Gly Leu Lys Arg Lys Thr Pro Ala Leu Lys Met Ser Val Ser 195 200 205 Lys Arg Ala Arg Lys Ala Ser Ser Asp Leu Asp Gln Ala Ser Val Ser 210 215 220 Pro Ser Glu Glu Glu Asn Ser Glu Ser Ser Ser Glu Ser Glu Lys Thr 225 230 235 240 Ser Asp Gln Asp Phe Thr Pro Glu Lys Lys Ala Ala Val Arg Ala Pro 245 250 255 Arg Arg Gly Pro Leu Gly Gly Arg Lys Lys Lys Lys Ala Pro Ser Ala 260 265 270 Ser Asp Ser Asp Ser Lys Ala Asp Ser Asp Gly Ala Lys Pro Glu Pro 275 280 285 Val Ala Met Ala Arg Ser Ala Ser Ser Ser Ser Ser Ser Ser Ser Ser 290 295 300 Ser Asp Ser Asp Val Ser Val Lys Lys Pro Pro Arg Gly Arg Lys Pro 305 310 315 320 Ala Glu Lys Pro Leu Pro Lys Pro Arg Gly Arg Lys Pro Lys Pro Glu 325 330 335 Arg Pro Pro Ser Ser Ser Ser Ser Asp Ser Asp Ser Asp Glu Val Asp 340 345 350 Arg Ile Ser Glu Trp Lys Arg Arg Asp Glu Ala Arg Arg Arg Glu Leu 355 360 365 Glu Ala Arg Arg Arg Arg Glu Gln Glu Glu Glu Leu Arg Arg Leu Arg 370 375 380 Glu Gln Glu Lys Glu Glu Lys Glu Arg Arg Arg Glu Arg Ala Asp Arg 385 390 395 400 Gly Glu Ala Glu Arg Gly Ser Gly Gly Ser Ser Gly Asp Glu Leu Arg 405 410 415 Glu Asp Asp Glu Pro Val Lys Lys Arg Gly Arg Lys Gly Arg Gly Arg 420 425 430 Gly Pro Pro Ser Ser Ser Asp Ser Glu Pro Glu Ala Glu Leu Glu Arg 435 440 445 Glu Ala Lys Lys Ser Ala Lys Lys Pro Gln Ser Ser Ser Thr Glu Pro 450 455 460 Ala Arg Lys Pro Gly Gln Lys Glu Lys Arg Val Arg Pro Glu Glu Lys 465 470 475 480 Gln Gln Ala Lys Pro Val Lys Val Glu Arg Thr Arg Lys Arg Ser Glu 485 490 495 Gly Phe Ser Met Asp Arg Lys Val Glu Lys Lys Lys Glu Pro Ser Val 500 505 510 Glu Glu Lys Leu Gln Lys Leu His Ser Glu Ile Lys Phe Ala Leu Lys 515 520 525 Val Asp Ser Pro Asp Val Lys Arg Cys Leu Asn Ala Leu Glu Glu Leu 530 535 540 Gly Thr Leu Gln Val Thr Ser Gln Ile Leu Gln Lys Asn Thr Asp Val 545 550 555 560 Val Ala Thr Leu Lys Lys Ile Arg Arg Tyr Lys Ala Asn Lys Asp Val 565 570 575 Met Glu Lys Ala Ala Glu Val Tyr Thr Arg Leu Lys Ser Arg Val Leu 580 585 590 Gly Pro Lys Ile Glu Ala Val Gln Lys Val Asn Lys Ala Gly Met Glu 595 600 605 Lys Glu Lys Ala Glu Glu Lys Leu Ala Gly Glu Glu Leu Ala Gly Glu 610 615 620 Glu Leu Ala Gly Glu Glu Ala Pro Gln Glu Lys Ala Glu Asp Lys Pro 625 630 635 640 Ser Thr Asp Leu Ser Ala Pro Val Asn Gly Glu Ala Thr Ser Gln Lys 645 650 655 Gly Glu Ser Ala Glu Asp Lys Glu His Glu Glu Gly Arg Asp Ser Glu 660 665 670 Glu Gly Pro Arg Cys Gly Ser Ser Glu Asp Leu His Asp Ser Val Arg 675 680 685 Glu Gly Pro Asp Leu Asp Arg Pro Gly Ser Asp Arg Gln Glu Arg Glu 690 695 700 Arg Ala Arg Gly Asp Ser Glu Ala Leu Asp Glu Glu Ser 705 710 715 30 288 PRT Homo sapiens 30 Met Phe Val Leu Leu Tyr Val Thr Ser Phe Ala Ile Cys Ala Ser Gly 1 5 10 15 Gln Pro Arg Gly Asn Gln Leu Lys Gly Glu Asn Tyr Ser Pro Arg Tyr 20 25 30 Ile Cys Ser Ile Pro Gly Leu Pro Gly Pro Pro Gly Pro Pro Gly Ala 35 40 45 Asn Gly Ser Pro Gly Pro His Gly Arg Ile Gly Leu Pro Gly Arg Asp 50 55 60 Gly Arg Asp Gly Arg Lys Gly Glu Lys Gly Glu Lys Gly Thr Ala Leu 65 70 75 80 Arg Gly Lys Thr Gly Pro Leu Gly Leu Ala Gly Glu Lys Gly Asp Gln 85 90 95 Gly Glu Thr Gly Lys Lys Gly Pro Ile Gly Pro Glu Gly Glu Lys Gly 100 105 110 Glu Val Gly Pro Ile Gly Pro Pro Gly Pro Lys Gly Asp Arg Gly Glu 115 120 125 Gln Gly Asp Pro Gly Leu Pro Gly Val Cys Arg Cys Gly Ser Ile Val 130 135 140 Leu Lys Ser Ala Phe Ser Val Gly Ile Thr Thr Ser Tyr Pro Glu Glu 145 150 155 160 Arg Leu Pro Ile Ile Phe Asn Lys Val Leu Phe Asn Glu Gly Glu His 165 170 175 Tyr Asn Pro Ala Thr Gly Lys Phe Ile Cys Ala Phe Pro Gly Ile Tyr 180 185 190 Tyr Phe Ser Tyr Asp Ile Thr Leu Ala Asn Lys His Leu Ala Ile Gly 195 200 205 Leu Val His Asn Gly Gln Tyr Arg Ile Lys Thr Phe Asp Ala Asn Thr 210 215 220 Gly Asn His Asp Val Ala Ser Gly Ser Thr Val Ile Tyr Leu Gln Pro 225 230 235 240 Glu Asp Glu Val Trp Leu Glu Ile Phe Phe Thr Asp Gln Asn Gly Leu 245 250 255 Phe Ser Asp Pro Gly Trp Ala Asp Ser Leu Phe Ser Gly Phe Leu Leu 260 265 270 Tyr Val Asp Thr Asp Tyr Leu Asp Ser Ile Ser Glu Asp Asp Glu Leu 275 280 285 31 303 PRT Homo sapiens 31 Met Gly Lys Glu Asp Thr Gln Glu Thr Arg Thr Glu Pro Lys Met Phe 1 5 10 15 Val Leu Leu Tyr Val Thr Ser Phe Ala Ile Cys Ala Ser Gly Gln Pro 20 25 30 Arg Gly Asn Gln Leu Lys Gly Glu Asn Tyr Ser Pro Arg Tyr Ile Cys 35 40 45 Ser Ile Pro Gly Leu Pro Gly Pro Pro Gly Pro Pro Gly Ala Asn Gly 50 55 60 Ser Pro Gly Pro His Gly Arg Ile Gly Leu Pro Gly Arg Asp Gly Arg 65 70 75 80 Asp Gly Arg Lys Gly Glu Lys Gly Glu Lys Gly Thr Ala Gly Leu Arg 85 90 95 Gly Lys Thr Gly Pro Leu Gly Leu Ala Gly Glu Lys Gly Asp Gln Gly 100 105 110 Glu Thr Gly Lys Lys Gly Pro Ile Gly Pro Glu Gly Glu Lys Gly Glu 115 120 125 Val Gly Pro Ile Gly Pro Pro Gly Pro Lys Gly Asp Arg Gly Glu Gln 130 135 140 Gly Asp Pro Gly Leu Pro Gly Val Cys Arg Cys Gly Ser Ile Val Leu 145 150 155 160 Lys Ser Ala Phe Ser Val Gly Ile Thr Thr Ser Tyr Pro Glu Glu Arg 165 170 175 Leu Pro Ile Ile Phe Asn Lys Val Leu Phe Asn Glu Gly Glu His Tyr 180 185 190 Asn Pro Ala Thr Gly Lys Phe Ile Cys Ala Phe Pro Gly Ile Tyr Tyr 195 200 205 Phe Ser Tyr Asp Ile Thr Leu Ala Asn Lys His Leu Ala Ile Gly Leu 210 215 220 Val His Asn Gly Gln Tyr Arg Ile Lys Thr Phe Asp Ala Asn Thr Gly 225 230 235 240 Asn His Asp Val Ala Ser Gly Ser Thr Val Ile Tyr Leu Gln Pro Glu 245 250 255 Asp Glu Val Trp Leu Glu Ile Phe Phe Thr Asp Gln Asn Gly Leu Phe 260 265 270 Ser Asp Pro Gly Trp Ala Asp Ser Leu Phe Ser Gly Phe Leu Leu Tyr 275 280 285 Val Asp Thr Asp Tyr Leu Asp Ser Ile Ser Glu Asp Asp Glu Leu 290 295 300 32 88 PRT Homo sapiens 32 Met Ser Leu Gln Ala Asp Phe Asp Met Val Thr Glu Asp Val Arg Lys 1 5 10 15 Leu Lys Thr Arg Pro Asp Asp Glu Glu Leu Lys Glu Leu Tyr Gly Leu 20 25 30 Tyr Lys Gln Ala Val Ile Gly Asn Ile Asn Ile Glu Cys Ser Glu Met 35 40 45 Leu Glu Leu Lys Gly Lys Ala Lys Trp Glu Ala Gln Asn Pro Gln Lys 50 55 60 Gly Leu Ser Glu Glu Asp Met Met Arg Ala Phe Ile Ser Lys Ala Glu 65 70 75 80 Glu Leu Ile Glu Lys Tyr Gly Ile 85 33 422 PRT Homo sapiens 33 Met His Gly Gly Ser Trp Gly Ser Val Cys Asp Asp Asp Trp Asp Val 1 5 10 15 Val Asp Ala Asn Val Val Cys Arg Gln Leu Gly Cys Gly Leu Ala Leu 20 25 30 Pro Val Pro Arg Pro Leu Ala Phe Gly Gln Gly Arg Gly Pro Ile Leu 35 40 45 Leu Asp Asn Val Glu Cys Arg Gly Gln Glu Ala Ala Leu Ser Glu Cys 50 55 60 Gly Ser Arg Gly Trp Gly Val His Asn Cys Phe His Tyr Glu Asp Val 65 70 75 80 Ala Val Leu Cys Asp Gly Glu Gly Ser Val Arg Leu Val Gly Gly Ala 85 90 95 Asn Leu Cys Gln Gly Arg Val Glu Ile Leu His Ser Gly Leu Trp Gly 100 105 110 Thr Val Cys Asp Asp Asp Trp Gly Leu Pro Asp Ala Ala Val Val Cys 115 120 125 Arg Gln Leu Gly Cys Gly Ala Ala Met Ala Ala Thr Thr Asn Ala Phe 130 135 140 Phe Gly Tyr Gly Thr Gly His Ile Leu Leu Asp Asn Val His Cys Glu 145 150 155 160 Gly Gly Glu Pro Arg Leu Ala Ala Cys Gln Ser Leu Gly Trp Gly Val 165 170 175 His Asn Cys Gly His His Glu Asp Ala Gly Ala Leu Cys Ala Gly Ala 180 185 190 Gly Ser Arg Gly Asp Gly Arg Gly Arg Gly Ser Pro Ser Gly Arg Gly 195 200 205 Pro Val Arg Pro Ala Gly Gly Arg Leu Arg Leu Val Gly Gly Pro Gly 210 215 220 Pro Cys Arg Gly Arg Val Glu Val Leu His Ala Gly Gly Trp Gly Thr 225 230 235 240 Val Cys Asp Asp Asp Trp Asp Phe Ala Asp Ala Arg Val Ala Cys Arg 245 250 255 Glu Ala Gly Cys Gly Pro Ala Leu Gly Ala Thr Gly Leu Gly His Phe 260 265 270 Gly Tyr Gly Arg Gly Pro Val Leu Leu Asp Asn Val Gly Cys Ala Gly 275 280 285 Thr Glu Ala Arg Leu Ser Asp Cys Phe His Leu Gly Trp Gly Gln His 290 295 300 Asn Cys Gly His His Glu Asp Ala Gly Ala Leu Cys Ala Gly His Leu 305 310 315 320 Arg Leu Val Asn Gly Ala His Arg Cys Glu Gly Arg Val Glu Leu Tyr 325 330 335 Leu Gly Gln Arg Trp Gly Thr Val Cys Asp Asp Ala Trp Asp Leu Arg 340 345 350 Ala Ala Gly Val Leu Cys Arg Gln Leu Gly Cys Gly Gln Ala Leu Ala 355 360 365 Ala Pro Gly Glu Ala His Phe Gly Pro Gly Arg Gly Pro Ile Leu Leu 370 375 380 Asp Asn Val Lys Cys Arg Gly Glu Glu Ser Ala Leu Leu Leu Cys Ser 385 390 395 400 His Ile Arg Trp Asp Ala His Asn Cys Asp His Ser Glu Asp Ala Ser 405 410 415 Val Leu Cys Gln Pro Ser 420 34 552 PRT Homo sapiens 34 Met Ala Thr Leu Pro Glu Lys Ala Leu Lys Glu Ala Trp Lys Gly Leu 1 5 10 15 Ile Pro Arg Phe Pro Trp Leu His Gly Lys Ala Glu Leu Arg Leu Val 20 25 30 Gly Gly Pro Ser Arg Cys Arg Gly Arg Leu Glu Val Met His Gly Gly 35 40 45 Ser Trp Gly Ser Val Cys Asp Asp Asp Trp Asp Val Val Asp Ala Asn 50 55 60 Val Val Cys Arg Gln Leu Gly Cys Gly Leu Ala Leu Pro Val Pro Arg 65 70 75 80 Pro Leu Ala Phe Gly Gln Gly Arg Gly Pro Ile Leu Leu Asp Asn Val 85 90 95 Glu Cys Arg Gly Gln Glu Ala Ala Leu Ser Glu Cys Gly Ser Arg Gly 100 105 110 Trp Gly Val His Asn Cys Phe His Tyr Glu Asp Val Ala Val Leu Cys 115 120 125 Asp Glu Phe Leu Pro Thr Gln Pro Pro Thr Arg Lys Met Leu Thr Ser 130 135 140 Arg Ala Pro Pro Thr Thr Leu Pro Asn Gly Lys Ser Glu Gly Ser Val 145 150 155 160 Arg Leu Val Gly Gly Ala Asn Leu Cys Gln Gly Arg Val Glu Ile Leu 165 170 175 His Ser Gly Leu Trp Gly Thr Val Cys Asp Asp Asp Trp Gly Leu Pro 180 185 190 Asp Ala Ala Val Val Cys Arg Gln Leu Gly Cys Gly Ala Ala Met Ala 195 200 205 Ala Thr Thr Asn Ala Phe Phe Gly Tyr Gly Thr Gly His Ile Leu Leu 210 215 220 Asp Asn Val His Cys Glu Gly Gly Glu Pro Arg Leu Ala Ala Cys Gln 225 230 235 240 Ser Leu Gly Trp Gly Val His Asn Cys Gly His His Glu Asp Ala Gly 245 250 255 Ala Leu Cys Ala Gly Leu Gly Pro Pro Thr Leu Thr Ala Leu Pro Ser 260 265 270 Ser Ala Thr Arg Glu Asp Trp Ala Trp Gln Thr Asp Pro Ser Ala Thr 275 280 285 Gly Val Gly Pro Gln Pro Ser Arg Glu Thr Ala Leu Leu Thr Thr Ala 290 295 300 Ala Trp Ala Ala Gly Lys Lys Ser Gly Arg Leu Arg Leu Val Gly Gly 305 310 315 320 Pro Gly Pro Cys Arg Gly Arg Val Glu Val Leu His Ala Gly Gly Trp 325 330 335 Gly Thr Val Cys Asp Asp Asp Trp Asp Phe Ala Asp Ala Arg Val Ala 340 345 350 Cys Arg Glu Ala Gly Cys Gly Pro Ala Leu Gly Ala Thr Gly Leu Gly 355 360 365 His Phe Gly Tyr Gly Arg Gly Pro Val Leu Leu Asp Asn Val Gly Cys 370 375 380 Ala Gly Thr Glu Ala Arg Leu Ser Asp Cys Phe His Leu Gly Trp Gly 385 390 395 400 Gln His Asn Cys Gly His His Glu Asp Ala Gly Ala Leu Cys Ala Gly 405 410 415 Glu Ala Asp Ser Glu Gly Pro Glu Glu Leu Gly Leu Gln Val Gln Gln 420 425 430 Asp Gly Ser Glu Thr Thr Arg Val Pro Thr Pro Arg Pro Arg Asp Gly 435 440 445 His Leu Arg Leu Val Asn Gly Ala His Arg Cys Glu Gly Arg Val Glu 450 455 460 Leu Tyr Leu Gly Gln Arg Trp Gly Thr Val Cys Asp Asp Ala Trp Asp 465 470 475 480 Leu Arg Ala Ala Gly Val Leu Cys Arg Gln Leu Gly Cys Gly Gln Ala 485 490 495 Leu Ala Ala Pro Gly Glu Ala His Phe Gly Pro Gly Arg Gly Pro Ile 500 505 510 Leu Leu Asp Asn Val Lys Cys Arg Gly Glu Glu Ser Ala Leu Leu Leu 515 520 525 Cys Ser His Ile Arg Trp Asp Ala His Asn Cys Asp His Ser Glu Asp 530 535 540 Ala Ser Val Leu Cys Gln Pro Ser 545 550 35 1709 PRT Homo sapiens 35 Met Gly Phe Leu Pro Lys Leu Leu Leu Leu Ala Ser Phe Phe Pro Ala 1 5 10 15 Gly Gln Ala Ser Trp Gly Val Ser Ser Pro Gln Asp Val Gln Gly Val 20 25 30 Lys Gly Ser Cys Leu Leu Ile Pro Cys Ile Phe Ser Phe Pro Ala Asp 35 40 45 Val Glu Val Pro Asp Gly Ile Thr Ala Ile Trp Tyr Tyr Asp Tyr Ser 50 55 60 Gly Gln Arg Gln Val Val Ser His Ser Ala Asp Pro Lys Leu Val Glu 65 70 75 80 Ala Arg Phe Arg Gly Arg Thr Glu Phe Met Gly Asn Pro Glu His Arg 85 90 95 Val Cys Asn Leu Leu Leu Lys Asp Leu Gln Pro Glu Asp Ser Gly Ser 100 105 110 Tyr Asn Phe Arg Phe Glu Ile Ser Glu Val Asn Arg Trp Ser Asp Val 115 120 125 Lys Gly Thr Leu Val Thr Val Thr Glu Glu Pro Arg Val Pro Thr Ile 130 135 140 Ala Ser Pro Val Glu Leu Leu Glu Gly Thr Glu Val Asp Phe Asn Cys 145 150 155 160 Ser Thr Pro Tyr Val Cys Leu Gln Glu Gln Val Arg Leu Gln Trp Gln 165 170 175 Gly Gln Asp Pro Ala Arg Ser Val Thr Phe Asn Ser Gln Lys Phe Glu 180 185 190 Pro Thr Gly Val Gly His Leu Glu Thr Leu His Met Ala Met Ser Trp 195 200 205 Gln Asp His Gly Arg Ile Leu Arg Cys Gln Leu Ser Val Ala Asn His 210 215 220 Arg Ala Gln Ser Glu Ile His Leu Gln Val Lys Tyr Ala Pro Lys Gly 225 230 235 240 Val Lys Ile Leu Leu Ser Pro Ser Gly Arg Asn Ile Leu Pro Gly Glu 245 250 255 Leu Val Thr Leu Thr Cys Gln Val Asn Ser Ser Tyr Pro Ala Val Ser 260 265 270 Ser Ile Lys Trp Leu Lys Asp Gly Val Arg Leu Gln Thr Lys Thr Gly 275 280 285 Val Leu His Leu Pro Gln Ala Ala Trp Ser Asp Ala Gly Val Tyr Thr 290 295 300 Cys Gln Ala Glu Asn Gly Val Gly Ser Leu Val Ser Pro Pro Ile Ser 305 310 315 320 Leu His Ile Phe Met Ala Glu Val Gln Val Ser Pro Ala Gly Pro Ile 325 330 335 Leu Glu Asn Gln Thr Val Thr Leu Val Cys Asn Thr Pro Asn Glu Ala 340 345 350 Pro Ser Asp Leu Arg Tyr Ser Trp Tyr Lys Asn His Val Leu Leu Glu 355 360 365 Asp Ala His Ser His Thr Leu Arg Leu His Leu Ala Thr Arg Ala Asp 370 375 380 Thr Gly Phe Tyr Phe Cys Glu Val Gln Asn Val His Gly Ser Glu Arg 385 390 395 400 Ser Gly Pro Val Ser Val Val Val Asn Leu Leu Thr Ala Phe Leu Glu 405 410 415 Thr Gln Ala Gly Leu Val Gly Ile Leu His Cys Ser Val Val Ser Glu 420 425 430 Pro Leu Ala Thr Leu Val Leu Ser His Gly Gly His Ile Leu Ala Ser 435 440 445 Thr Ser Gly Asp Ser Asp His Ser Pro Arg Phe Ser Gly Thr Ser Gly 450 455 460 Pro Asn Ser Leu Arg Leu Glu Ile Arg Asp Leu Glu Glu Thr Asp Ser 465 470 475 480 Gly Glu Tyr Lys Cys Ser Ala Thr Asn Ser Leu Gly Asn Ala Thr Ser 485 490 495 Thr Leu Asp Phe His Ala Asn Ala Ala Arg Leu Leu Ile Ser Pro Ala 500 505 510 Ala Glu Val Val Glu Gly Gln Ala Val Thr Leu Ser Cys Arg Ser Gly 515 520 525 Leu Ser Pro Thr Pro Asp Ala Arg Phe Ser Trp Tyr Leu Asn Gly Ala 530 535 540 Leu Leu His Glu Gly Pro Gly Ser Ser Leu Leu Leu Pro Ala Ala Ser 545 550 555 560 Ser Thr Asp Ala Gly Ser Tyr His Cys Arg Ala Arg Asp Gly His Ser 565 570 575 Ala Ser Gly Pro Ser Ser Pro Ala Val Leu Thr Val Leu Tyr Pro Pro 580 585 590 Arg Gln Pro Thr Phe Thr Thr Arg Leu Asp Leu Asp Ala Ala Gly Ala 595 600 605 Gly Ala Gly Arg Arg Gly Leu Leu Leu Cys Arg Val Asp Ser Asp Pro 610 615 620 Pro Ala Arg Leu Gln Leu Leu His Lys Asp Arg Val Val Ala Thr Ser 625 630 635 640 Leu Pro Ser Gly Gly Gly Cys Ser Thr Cys Gly Gly Cys Ser Pro Arg 645 650 655 Met Lys Val Thr Lys Ala Pro Asn Leu Leu Arg Val Glu Ile His Asn 660 665 670 Pro Leu Leu Glu Glu Glu Gly Leu Tyr Leu Cys Glu Ala Ser Asn Ala 675 680 685 Leu Gly Asn Ala Ser Thr Ser Ala Thr Phe Asn Gly Gln Ala Thr Val 690 695 700 Leu Ala Ile Ala Pro Ser His Thr Leu Gln Glu Gly Thr Glu Ala Asn 705 710 715 720 Leu Thr Cys Asn Val Ser Arg Glu Ala Ala Gly Ser Pro Ala Asn Phe 725 730 735 Ser Trp Phe Arg Asn Gly Val Leu Trp Ala Gln Gly Pro Leu Glu Thr 740 745 750 Val Thr Leu Leu Pro Val Ala Arg Thr Asp Ala Ala Leu Tyr Ala Cys 755 760 765 Arg Ile Leu Thr Glu Ala Gly Ala Gln Leu Ser Thr Pro Val Leu Leu 770 775 780 Ser Val Leu Tyr Pro Pro Asp Arg Pro Lys Leu Ser Ala Leu Leu Asp 785 790 795 800 Met Gly Gln Gly His Met Ala Leu Phe Ile Cys Thr Val Asp Ser Arg 805 810 815 Pro Leu Ala Leu Leu Ala Leu Phe His Gly Glu His Leu Leu Ala Thr 820 825 830 Ser Leu Gly Pro Gln Val Pro Ser His Gly Arg Phe Gln Ala Lys Ala 835 840 845 Glu Ala Asn Ser Leu Lys Leu Glu Val Arg Glu Leu Gly Leu Gly Asp 850 855 860 Ser Gly Ser Tyr Arg Cys Glu Ala Thr Asn Val Leu Gly Ser Ser Asn 865 870 875 880 Thr Ser Leu Phe Phe Gln Val Arg Gly Ala Trp Val Gln Val Ser Pro 885 890 895 Ser Pro Glu Leu Gln Glu Gly Gln Ala Val Val Leu Ser Cys Gln Val 900 905 910 His Thr Gly Val Pro Glu Gly Thr Ser Tyr Arg Trp Tyr Arg Asp Gly 915 920 925 Gln Pro Leu Gln Glu Ser Thr Ser Ala Thr Leu Arg Phe Ala Ala Ile 930 935 940 Thr Leu Thr Gln Ala Gly Ala Tyr His Cys Gln Ala Gln Ala Pro Gly 945 950 955 960 Ser Ala Thr Thr Ser Leu Ala Ala Pro Ile Ser Leu His Val Ser Tyr 965 970 975 Ala Pro Arg His Val Thr Leu Thr Thr Leu Met Asp Thr Gly Pro Gly 980 985 990 Arg Leu Gly Leu Leu Leu Cys Arg Val Asp Ser Asp Pro Pro Ala Gln 995 1000 1005 Leu Arg Leu Leu His Gly Asp Arg Leu Val Ala Ser Thr Leu Gln Gly 1010 1015 1020 Val Gly Gly Pro Glu Gly Ser Ser Pro Arg Leu His Val Ala Val Ala 1025 1030 1035 1040 Pro Asn Thr Leu Arg Leu Glu Ile His Gly Ala Met Leu Glu Asp Glu 1045 1050 1055 Gly Val Tyr Ile Cys Glu Ala Ser Asn Thr Leu Gly Gln Ala Ser Ala 1060 1065 1070 Ser Ala Asp Phe Asp Ala Gln Ala Val Asn Val Gln Val Trp Pro Gly 1075 1080 1085 Ala Thr Val Arg Glu Gly Gln Leu Val Asn Leu Thr Cys Leu Val Trp 1090 1095 1100 Thr Thr His Pro Ala Gln Leu Thr Tyr Thr Trp Tyr Gln Asp Gly Gln 1105 1110 1115 1120 Gln Arg Leu Asp Ala His Ser Ile Pro Leu Pro Asn Val Thr Val Arg 1125 1130 1135 Asp Ala Thr Ser Tyr Arg Cys Gly Val Gly Pro Pro Gly Arg Ala Pro 1140 1145 1150 Arg Leu Ser Arg Pro Ile Thr Leu Asp Val Leu Tyr Ala Pro Arg Asn 1155 1160 1165 Leu Arg Leu Thr Tyr Leu Leu Glu Ser His Gly Gly Gln Leu Ala Leu 1170 1175 1180 Val Leu Cys Thr Val Asp Ser Arg Pro Pro Ala Gln Leu Ala Leu Ser 1185 1190 1195 1200 His Ala Gly Arg Leu Leu Ala Ser Ser Thr Ala Ala Ser Val Pro Asn 1205 1210 1215 Thr Leu Arg Leu Glu Leu Arg Gly Pro Gln Pro Arg Asp Glu Gly Phe 1220 1225 1230 Tyr Ser Cys Ser Ala Arg Ser Pro Leu Gly Gln Ala Asn Thr Ser Leu 1235 1240 1245 Glu Leu Arg Leu Glu Gly Val Arg Val Ile Leu Ala Pro Glu Ala Ala 1250 1255 1260 Val Pro Glu Gly Ala Pro Ile Thr Val Thr Cys Ala Asp Pro Ala Ala 1265 1270 1275 1280 His Ala Pro Thr Leu Tyr Thr Trp Tyr His Asn Gly Arg Trp Leu Gln 1285 1290 1295 Glu Gly Pro Ala Ala Ser Leu Ser Phe Leu Val Ala Thr Arg Ala His 1300 1305 1310 Ala Gly Ala Tyr Ser Cys Gln Ala Gln Asp Ala Gln Gly Thr Arg Ser 1315 1320 1325 Ser Arg Pro Ala Ala Leu Gln Val Leu Tyr Ala Pro Gln Asp Ala Val 1330 1335 1340 Leu Ser Ser Phe Arg Asp Ser Arg Ala Arg Ser Met Ala Val Ile Gln 1345 1350 1355 1360 Cys Thr Val Asp Ser Glu Pro Pro Ala Glu Leu Ala Leu Ser His Asp 1365 1370 1375 Gly Lys Val Leu Ala Thr Ser Ser Gly Val His Ser Leu Ala Ser Gly 1380 1385 1390 Thr Gly His Val Gln Val Ala Arg Asn Ala Leu Arg Leu Gln Val Gln 1395 1400 1405 Asp Val Pro Ala Gly Asp Asp Thr Tyr Val Cys Thr Ala Gln Asn Leu 1410 1415 1420 Leu Gly Ser Ile Ser Thr Ile Gly Arg Leu Gln Val Glu Gly Ala Arg 1425 1430 1435 1440 Val Val Ala Glu Pro Gly Leu Asp Val Pro Glu Gly Ala Ala Leu Asn 1445 1450 1455 Leu Ser Cys Arg Leu Leu Gly Gly Pro Gly Pro Val Gly Asn Ser Thr 1460 1465 1470 Phe Ala Trp Phe Trp Asn Asp Arg Arg Leu His Ala Glu Pro Val Pro 1475 1480 1485 Thr Leu Ala Phe Thr His Val Ala Arg Ala Gln Ala Gly Met Tyr His 1490 1495 1500 Cys Leu Ala Glu Leu Pro Thr Gly Ala Ala Ala Ser Ala Pro Val Met 1505 1510 1515 1520 Leu Arg Val Leu Tyr Pro Pro Lys Thr Pro Thr Met Met Val Phe Val 1525 1530 1535 Glu Pro Glu Gly Gly Leu Arg Gly Ile Leu Asp Cys Arg Val Asp Ser 1540 1545 1550 Glu Pro Leu Ala Ser Leu Thr Leu His Leu Gly Ser Arg Leu Val Ala 1555 1560 1565 Ser Ser Gln Pro Gln Gly Ala Pro Ala Glu Pro His Ile His Val Leu 1570 1575 1580 Ala Ser Pro Asn Ala Leu Arg Val Asp Ile Glu Ala Leu Arg Pro Ser 1585 1590 1595 1600 Asp Gln Gly Glu Tyr Ile Cys Ser Ala Ser Asn Val Leu Gly Ser Ala 1605 1610 1615 Ser Thr Ser Thr Tyr Phe Gly Val Arg Ala Leu His Arg Leu His Gln 1620 1625 1630 Phe Gln Gln Leu Leu Trp Val Leu Gly Leu Leu Val Gly Leu Leu Leu 1635 1640 1645 Leu Leu Leu Gly Leu Gly Ala Cys Tyr Thr Trp Arg Arg Arg Arg Val 1650 1655 1660 Cys Lys Gln Ser Met Gly Glu Asn Ser Val Glu Met Ala Phe Gln Lys 1665 1670 1675 1680 Glu Thr Thr Gln Gly Phe Leu Cys Gly Lys Leu Ile Asp Pro Asp Ala 1685 1690 1695 Ala Thr Cys Glu Thr Ser Thr Cys Ala Pro Pro Leu Gly 1700 1705 36 1694 PRT Homo sapiens 36 Met Gly Phe Leu Pro Lys Leu Leu Leu Leu Ala Ser Phe Phe Pro Ala 1 5 10 15 Gly Gln Ala Ser Trp Gly Val Ser Ser Pro Gln Asp Val Gln Gly Val 20 25 30 Lys Gly Ser Cys Leu Leu Ile Pro Cys Ile Phe Ser Phe Pro Ala Asp 35 40 45 Val Glu Val Pro Asp Gly Ile Thr Ala Ile Trp Tyr Tyr Asp Tyr Ser 50 55 60 Gly Gln Arg Gln Val Val Ser His Ser Ala Asp Pro Lys Leu Val Glu 65 70 75 80 Ala Arg Phe Arg Gly Arg Thr Glu Phe Met Gly Asn Pro Glu His Arg 85 90 95 Val Cys Asn Leu Leu Leu Lys Asp Leu Gln Pro Glu Asp Ser Gly Ser 100 105 110 Tyr Asn Phe Arg Phe Glu Ile Ser Glu Val Asn Arg Trp Ser Asp Val 115 120 125 Lys Gly Thr Leu Val Thr Val Thr Glu Glu Pro Arg Val Pro Thr Ile 130 135 140 Ala Ser Pro Val Glu Leu Leu Glu Gly Thr Glu Val Asp Phe Asn Cys 145 150 155 160 Ser Thr Pro Tyr Val Cys Leu Gln Glu Gln Val Arg Leu Gln Trp Gln 165 170 175 Gly Gln Asp Pro Ala Arg Ser Val Thr Phe Asn Ser Gln Lys Phe Glu 180 185 190 Pro Thr Gly Val Gly His Leu Glu Thr Leu His Met Ala Met Ser Trp 195 200 205 Gln Asp His Gly Arg Ile Leu Arg Cys Gln Leu Ser Val Ala Asn His 210 215 220 Arg Ala Gln Ser Glu Ile His Leu Gln Val Lys Tyr Ala Pro Lys Gly 225 230 235 240 Val Lys Ile Leu Leu Ser Pro Ser Gly Arg Asn Ile Leu Pro Gly Glu 245 250 255 Leu Val Thr Leu Thr Cys Gln Val Asn Ser Ser Tyr Pro Ala Val Ser 260 265 270 Ser Ile Lys Trp Leu Lys Asp Gly Val Arg Leu Gln Thr Lys Thr Gly 275 280 285 Val Leu His Leu Pro Gln Ala Ala Trp Ser Asp Ala Gly Val Tyr Thr 290 295 300 Cys Gln Ala Glu Asn Gly Val Gly Ser Leu Val Ser Pro Pro Ile Ser 305 310 315 320 Leu His Ile Phe Met Ala Glu Val Gln Val Ser Pro Ala Gly Pro Ile 325 330 335 Leu Glu Asn Gln Thr Val Thr Leu Val Cys Asn Thr Pro Asn Glu Ala 340 345 350 Pro Ser Asp Leu Arg Tyr Ser Trp Tyr Lys Asn His Val Leu Leu Glu 355 360 365 Asp Ala His Ser His Thr Leu Arg Leu His Leu Ala Thr Arg Ala Asp 370 375 380 Thr Gly Phe Tyr Phe Cys Glu Val Gln Asn Val His Gly Ser Glu Arg 385 390 395 400 Ser Gly Pro Val Ser Val Val Val Asn Leu Leu Thr Ala Phe Leu Glu 405 410 415 Thr Gln Ala Gly Leu Val Gly Ile Leu His Cys Ser Val Val Ser Glu 420 425 430 Pro Leu Ala Thr Leu Val Leu Ser His Gly Gly His Ile Leu Ala Ser 435 440 445 Thr Ser Gly Asp Ser Asp His Ser Pro Arg Phe Ser Gly Thr Ser Gly 450 455 460 Pro Asn Ser Leu Arg Leu Glu Ile Arg Asp Leu Glu Glu Thr Asp Ser 465 470 475 480 Gly Glu Tyr Lys Cys Ser Ala Thr Asn Ser Leu Gly Asn Ala Thr Ser 485 490 495 Thr Leu Asp Phe His Ala Asn Ala Ala Arg Leu Leu Ile Ser Pro Ala 500 505 510 Ala Glu Val Val Glu Gly Gln Ala Val Thr Leu Ser Cys Arg Ser Gly 515 520 525 Leu Ser Pro Thr Pro Asp Ala Arg Phe Ser Trp Tyr Leu Asn Gly Ala 530 535 540 Leu Leu His Glu Gly Pro Gly Ser Ser Leu Leu Leu Pro Ala Ala Ser 545 550 555 560 Ser Thr Asp Ala Gly Ser Tyr His Cys Arg Ala Arg Asp Gly His Ser 565 570 575 Ala Ser Gly Pro Ser Ser Pro Ala Val Leu Thr Val Leu Tyr Pro Pro 580 585 590 Arg Gln Pro Thr Phe Thr Thr Arg Leu Asp Leu Asp Ala Ala Gly Ala 595 600 605 Gly Ala Gly Arg Arg Gly Leu Leu Leu Cys Arg Val Asp Ser Asp Pro 610 615 620 Pro Ala Arg Leu Gln Leu Leu His Lys Asp Arg Val Val Ala Thr Ser 625 630 635 640 Leu Pro Ser Gly Gly Gly Cys Ser Thr Cys Gly Gly Cys Ser Pro Arg 645 650 655 Met Lys Val Thr Lys Ala Pro Asn Leu Leu Arg Val Glu Ile His Asn 660 665 670 Pro Leu Leu Glu Glu Glu Gly Leu Tyr Leu Cys Glu Ala Ser Asn Ala 675 680 685 Leu Gly Asn Ala Ser Thr Ser Ala Thr Phe Asn Gly Gln Ala Thr Val 690 695 700 Leu Ala Ile Ala Pro Ser His Thr Leu Gln Glu Gly Thr Glu Ala Asn 705 710 715 720 Leu Thr Cys Asn Val Ser Arg Glu Ala Ala Gly Ser Pro Ala Asn Phe 725 730 735 Ser Trp Phe Arg Asn Gly Val Leu Trp Ala Gln Gly Pro Leu Glu Thr 740 745 750 Val Thr Leu Leu Pro Val Ala Arg Thr Asp Ala Ala Leu Tyr Ala Cys 755 760 765 Arg Ile Leu Thr Glu Ala Gly Ala Gln Leu Ser Thr Pro Val Leu Leu 770 775 780 Ser Val Leu Tyr Pro Pro Asp Arg Pro Lys Leu Ser Ala Leu Leu Asp 785 790 795 800 Met Gly Gln Gly His Met Ala Leu Phe Ile Cys Thr Val Asp Ser Arg 805 810 815 Pro Leu Ala Leu Leu Ala Leu Phe His Gly Glu His Leu Leu Ala Thr 820 825 830 Ser Leu Gly Pro Gln Val Pro Ser His Gly Arg Phe Gln Ala Lys Ala 835 840 845 Glu Ala Asn Ser Leu Lys Leu Glu Val Arg Glu Leu Gly Leu Gly Asp 850 855 860 Ser Gly Ser Tyr Arg Cys Glu Ala Thr Asn Val Leu Gly Ser Ser Asn 865 870 875 880 Thr Ser Leu Phe Phe Gln Val Arg Gly Ala Trp Val Gln Val Ser Pro 885 890 895 Ser Pro Glu Leu Gln Glu Gly Gln Ala Val Val Leu Ser Cys Gln Val 900 905 910 His Thr Gly Val Pro Glu Gly Thr Ser Tyr Arg Trp Tyr Arg Asp Gly 915 920 925 Gln Pro Leu Gln Glu Ser Thr Ser Ala Thr Leu Arg Phe Ala Ala Ile 930 935 940 Thr Leu Thr Gln Ala Gly Ala Tyr His Cys Gln Ala Gln Ala Pro Gly 945 950 955 960 Ser Ala Thr Thr Ser Leu Ala Ala Pro Ile Ser Leu His Val Ser Tyr 965 970 975 Ala Pro Arg His Val Thr Leu Thr Thr Leu Met Asp Thr Gly Pro Gly 980 985 990 Arg Leu Gly Leu Leu Leu Cys Arg Val Asp Ser Asp Pro Pro Ala Gln 995 1000 1005 Leu Arg Leu Leu His Gly Asp Arg Leu Val Ala Ser Thr Leu Gln Gly 1010 1015 1020 Val Gly Gly Pro Glu Gly Ser Ser Pro Arg Leu His Val Ala Val Ala 1025 1030 1035 1040 Pro Asn Thr Leu Arg Leu Glu Ile His Gly Ala Met Leu Glu Asp Glu 1045 1050 1055 Gly Val Tyr Ile Cys Glu Ala Ser Asn Thr Leu Gly Gln Ala Ser Ala 1060 1065 1070 Ser Ala Asp Phe Asp Ala Gln Ala Val Asn Val Gln Val Trp Pro Gly 1075 1080 1085 Ala Thr Val Arg Glu Gly Gln Leu Val Asn Leu Thr Cys Leu Val Trp 1090 1095 1100 Thr Thr His Pro Ala Gln Leu Thr Tyr Thr Trp Tyr Gln Asp Gly Gln 1105 1110 1115 1120 Gln Arg Leu Asp Ala His Ser Ile Pro Leu Pro Asn Val Thr Val Arg 1125 1130 1135 Asp Ala Thr Ser Tyr Arg Cys Gly Val Gly Pro Pro Gly Arg Ala Pro 1140 1145 1150 Arg Leu Ser Arg Pro Ile Thr Leu Asp Val Leu Tyr Ala Pro Arg Asn 1155 1160 1165 Leu Arg Leu Thr Tyr Leu Leu Glu Ser His Gly Gly Gln Leu Ala Leu 1170 1175 1180 Val Leu Cys Thr Val Asp Ser Arg Pro Pro Ala Gln Leu Ala Leu Ser 1185 1190 1195 1200 His Ala Gly Arg Leu Leu Ala Ser Ser Thr Ala Ala Ser Val Pro Asn 1205 1210 1215 Thr Leu Arg Leu Glu Leu Arg Gly Pro Gln Pro Arg Asp Glu Gly Phe 1220 1225 1230 Tyr Ser Cys Ser Ala Arg Ser Pro Leu Gly Gln Ala Asn Thr Ser Leu 1235 1240 1245 Glu Leu Arg Leu Glu Gly Val Arg Val Ile Leu Ala Pro Glu Ala Ala 1250 1255 1260 Val Pro Glu Gly Ala Pro Ile Thr Val Thr Cys Ala Asp Pro Ala Ala 1265 1270 1275 1280 His Ala Pro Thr Leu Tyr Thr Trp Tyr His Asn Gly Arg Trp Leu Gln 1285 1290 1295 Glu Gly Pro Ala Ala Ser Leu Ser Phe Leu Val Ala Thr Arg Ala His 1300 1305 1310 Ala Gly Ala Tyr Ser Cys Gln Ala Gln Asp Ala Gln Gly Thr Arg Ser 1315 1320 1325 Ser Arg Pro Ala Ala Leu Gln Val Leu Tyr Ala Pro Gln Asp Ala Val 1330 1335 1340 Leu Ser Ser Phe Arg Asp Ser Arg Ala Arg Ser Met Ala Val Ile Gln 1345 1350 1355 1360 Cys Thr Val Asp Ser Glu Pro Pro Ala Glu Leu Ala Leu Ser His Asp 1365 1370 1375 Gly Lys Val Leu Ala Thr Ser Ser Gly Val His Ser Leu Ala Ser Gly 1380 1385 1390 Thr Gly His Val Gln Val Ala Arg Asn Ala Leu Arg Leu Gln Val Gln 1395 1400 1405 Asp Val Pro Ala Gly Asp Asp Thr Tyr Val Cys Thr Ala Gln Asn Leu 1410 1415 1420 Leu Gly Ser Ile Ser Thr Ile Gly Arg Leu Gln Val Glu Gly Ala Arg 1425 1430 1435 1440 Val Val Ala Glu Pro Gly Leu Asp Val Pro Glu Gly Ala Ala Leu Asn 1445 1450 1455 Leu Ser Cys Arg Leu Leu Gly Gly Pro Gly Pro Val Gly Asn Ser Thr 1460 1465 1470 Phe Ala Trp Phe Trp Asn Asp Arg Arg Leu His Ala Glu Pro Val Pro 1475 1480 1485 Thr Leu Ala Phe Thr His Val Ala Arg Ala Gln Ala Gly Met Tyr His 1490 1495 1500 Cys Leu Ala Glu Leu Pro Thr Gly Ala Ala Ala Ser Ala Pro Val Met 1505 1510 1515 1520 Leu Arg Val Leu Tyr Pro Pro Lys Thr Pro Thr Met Met Val Phe Val 1525 1530 1535 Glu Pro Glu Gly Gly Leu Arg Gly Ile Leu Asp Cys Arg Val Asp Ser 1540 1545 1550 Glu Pro Leu Ala Ser Leu Thr Leu His Leu Gly Ser Arg Leu Val Ala 1555 1560 1565 Ser Ser Gln Pro Gln Gly Ala Pro Ala Glu Pro His Ile His Val Leu 1570 1575 1580 Ala Ser Pro Asn Ala Leu Arg Val Asp Ile Glu Ala Leu Arg Pro Ser 1585 1590 1595 1600 Asp Gln Gly Glu Tyr Ile Cys Ser Ala Ser Asn Val Leu Gly Ser Ala 1605 1610 1615 Ser Thr Ser Thr Tyr Phe Gly Val Arg Ala Leu His Arg Leu His Gln 1620 1625 1630 Phe Gln Gln Leu Leu Trp Val Leu Gly Leu Leu Val Gly Leu Leu Leu 1635 1640 1645 Leu Leu Leu Gly Leu Gly Ala Cys Tyr Thr Trp Arg Asp Trp Val Leu 1650 1655 1660 Pro Tyr Trp Pro Leu Gln Glu Trp Arg Ala Asp Thr Asp Val Val Ser 1665 1670 1675 1680 Ile Leu Ile Pro Ala Pro Asp Ala Ser Leu Phe Met Thr Val 1685 1690 37 745 PRT Homo sapiens 37 Met Phe Pro Leu Arg Ala Leu Trp Leu Val Trp Ala Leu Leu Gly Val 1 5 10 15 Ala Gly Ser Cys Pro Glu Pro Cys Ala Cys Val Asp Lys Tyr Ala His 20 25 30 Gln Phe Ala Asp Cys Ala Tyr Lys Glu Leu Arg Glu Val Pro Glu Gly 35 40 45 Leu Pro Ala Asn Val Thr Thr Leu Ser Leu Ser Ala Asn Lys Ile Thr 50 55 60 Val Leu Arg Arg Gly Ala Phe Ala Asp Val Thr Gln Val Thr Ser Leu 65 70 75 80 Trp Leu Ala His Asn Glu Val Arg Thr Val Glu Pro Gly Ala Leu Ala 85 90 95 Val Leu Ser Gln Leu Lys Asn Leu Asp Leu Ser His Asn Phe Ile Ser 100 105 110 Ser Phe Pro Trp Ser Asp Leu Arg Asn Leu Ser Ala Leu Gln Leu Leu 115 120 125 Lys Met Asn His Asn Arg Leu Gly Ser Leu Pro Arg Asp Ala Leu Gly 130 135 140 Ala Leu Pro Asp Leu Arg Ser Leu Arg Ile Asn Asn Asn Arg Leu Arg 145 150 155 160 Thr Leu Ala Pro Gly Thr Phe Asp Ala Leu Ser Ala Leu Ser His Leu 165 170 175 Gln Leu Tyr His Asn Pro Phe His Cys Gly Cys Gly Leu Val Trp Leu 180 185 190 Gln Ala Trp Ala Ala Ser Thr Arg Val Ser Leu Pro Glu Pro Asp Ser 195 200 205 Ile Ala Cys Ala Ser Pro Pro Ala Leu Gln Gly Val Pro Val Tyr Arg 210 215 220 Leu Pro Ala Leu Pro Cys Ala Pro Pro Ser Val His Leu Ser Ala Glu 225 230 235 240 Pro Pro Leu Glu Ala Pro Gly Thr Pro Leu Arg Ala Gly Leu Ala Phe 245 250 255 Val Leu His Cys Ile Ala Asp Gly His Pro Thr Pro Arg Leu Gln Trp 260 265 270 Gln Leu Gln Ile Pro Gly Gly Thr Val Val Leu Glu Pro Pro Val Leu 275 280 285 Ser Gly Glu Asp Asp Gly Val Gly Ala Glu Glu Gly Glu Gly Glu Gly 290 295 300 Asp Gly Asp Leu Leu Thr Gln Thr Gln Ala Gln Thr Pro Thr Pro Ala 305 310 315 320 Pro Ala Trp Pro Ala Pro Pro Ala Thr Pro Arg Phe Leu Ala Leu Ala 325 330 335 Asn Gly Ser Leu Leu Val Pro Leu Leu Ser Ala Lys Glu Ala Gly Val 340 345 350 Tyr Thr Cys Arg Ala His Asn Glu Leu Gly Ala Asn Ser Thr Ser Ile 355 360 365 Arg Val Ala Val Ala Ala Thr Gly Pro Pro Lys His Ala Pro Gly Ala 370 375 380 Gly Gly Glu Pro Asp Gly Gln Ala Pro Thr Ser Glu Arg Lys Ser Thr 385 390 395 400 Ala Lys Gly Arg Gly Asn Ser Val Leu Pro Ser Lys Pro Glu Gly Lys 405 410 415 Ile Lys Gly Gln Gly Leu Ala Lys Val Ser Ile Leu Gly Glu Thr Glu 420 425 430 Thr Glu Pro Glu Glu Asp Thr Ser Glu Gly Glu Glu Ala Glu Asp Gln 435 440 445 Ile Leu Ala Asp Pro Ala Glu Glu Gln Arg Cys Gly Asn Gly Asp Pro 450 455 460 Ser Arg Tyr Val Ser Asn His Ala Phe Asn Gln Ser Ala Glu Leu Lys 465 470 475 480 Pro His Val Phe Glu Leu Gly Val Ile Ala Leu Asp Val Ala Glu Arg 485 490 495 Glu Ala Arg Val Gln Leu Thr Pro Leu Ala Ala Arg Trp Gly Pro Gly 500 505 510 Pro Gly Gly Ala Gly Gly Ala Pro Arg Pro Gly Arg Arg Pro Leu Arg 515 520 525 Leu Leu Tyr Leu Cys Pro Ala Gly Gly Gly Ala Ala Val Gln Trp Ser 530 535 540 Arg Val Glu Glu Gly Val Asn Ala Tyr Trp Phe Arg Gly Leu Arg Pro 545 550 555 560 Gly Thr Asn Tyr Ser Val Cys Leu Ala Leu Ala Gly Glu Ala Cys His 565 570 575 Val Gln Val Val Phe Ser Thr Lys Lys Glu Leu Pro Ser Leu Leu Val 580 585 590 Ile Val Ala Val Ser Val Phe Leu Leu Val Leu Ala Thr Val Pro Leu 595 600 605 Leu Gly Ala Ala Cys Cys His Leu Leu Ala Lys His Pro Gly Lys Pro 610 615 620 Tyr Arg Leu Ile Leu Arg Pro Gln Ala Pro Asp Pro Met Glu Lys Arg 625 630 635 640 Ile Ala Ala Asp Phe Asp Pro Arg Ala Ser Tyr Leu Glu Ser Glu Lys 645 650 655 Ser Tyr Pro Ala Gly Gly Glu Ala Gly Gly Glu Glu Pro Glu Asp Val 660 665 670 Gln Gly Glu Gly Leu Asp Glu Asp Ala Glu Gln Gly Asp Pro Ser Gly 675 680 685 Asp Leu Gln Arg Glu Glu Ser Leu Ala Ala Cys Ser Leu Val Glu Ser 690 695 700 Gln Ser Lys Ala Asn Gln Glu Glu Phe Glu Ala Gly Ser Glu Tyr Ser 705 710 715 720 Asp Arg Leu Pro Leu Gly Ala Glu Ala Val Asn Ile Ala Gln Glu Ile 725 730 735 Asn Gly Asn Tyr Arg Gln Thr Ala Gly 740 745 38 251 PRT Homo sapiens 38 Met Ser Ala Tyr Gly Met Pro Met Tyr Lys Ser Gly Asp Leu Val Phe 1 5 10 15 Ala Lys Leu Lys Gly Tyr Ala His Trp Pro Ala Arg Ile Glu His Met 20 25 30 Thr Gln Pro Asn Arg Tyr Gln Val Phe Phe Phe Gly Thr His Glu Thr 35 40 45 Ala Phe Leu Ser Pro Lys Arg Leu Phe Pro Tyr Lys Glu Cys Lys Glu 50 55 60 Lys Phe Gly Lys Pro Asn Lys Arg Arg Gly Phe Ser Ala Gly Leu Trp 65 70 75 80 Glu Ile Glu Asn Asn Pro Thr Val Gln Ala Ser Asp Cys Pro Leu Ala 85 90 95 Ser Glu Lys Gly Ser Gly Asp Gly Pro Trp Pro Glu Pro Glu Ala Ala 100 105 110 Glu Gly Asp Glu Asp Lys Pro Thr His Ala Gly Gly Gly Gly Asp Glu 115 120 125 Leu Gly Lys Pro Asp Asp Asp Lys Pro Thr Glu Glu Glu Lys Gly Pro 130 135 140 Leu Lys Arg Ser Ala Gly Asp Pro Pro Glu Asp Ala Pro Lys Arg Pro 145 150 155 160 Lys Glu Ala Ala Pro Asp Gln Glu Glu Glu Ala Glu Ala Glu Arg Ala 165 170 175 Ala Glu Ala Glu Arg Ala Ala Ala Ala Ala Ala Ala Thr Ala Val Asp 180 185 190 Glu Glu Ser Pro Phe Leu Val Ala Val Glu Asn Gly Ser Ala Pro Ser 195 200 205 Glu Pro Gly Leu Val Cys Glu Pro Pro Gln Pro Glu Glu Glu Glu Leu 210 215 220 Arg Glu Glu Glu Val Ala Asp Glu Glu Ala Ser Gln Glu Trp His Ala 225 230 235 240 Glu Ala Pro Gly Gly Gly Asp Arg Asp Ser Leu 245 250 39 408 PRT Homo sapiens 39 Phe Leu Ile Ser Asp Arg Asp Pro Gln Cys Asn Leu His Cys Ser Arg 1 5 10 15 Thr Gln Pro Lys Pro Ile Cys Ala Ser Asp Gly Arg Ser Tyr Glu Ser 20 25 30 Met Cys Glu Tyr Gln Arg Ala Lys Cys Arg Asp Pro Thr Leu Gly Val 35 40 45 Val His Arg Gly Arg Cys Lys Asp Ala Gly Gln Ser Lys Cys Arg Leu 50 55 60 Glu Arg Ala Gln Ala Leu Glu Gln Ala Lys Lys Pro Gln Glu Ala Val 65 70 75 80 Phe Val Pro Glu Cys Gly Glu Asp Gly Ser Phe Thr Gln Val Gln Cys 85 90 95 His Thr Tyr Thr Gly Tyr Cys Trp Cys Val Thr Pro Asp Gly Lys Pro 100 105 110 Ile Ser Gly Ser Ser Val Gln Asn Lys Thr Pro Val Cys Ser Gly Ser 115 120 125 Val Thr Asp Lys Pro Leu Ser Gln Gly Asn Ser Gly Arg Lys Asp Asp 130 135 140 Gly Ser Lys Pro Thr Pro Thr Met Glu Thr Gln Pro Val Phe Asp Gly 145 150 155 160 Asp Glu Ile Thr Ala Pro Thr Leu Trp Ile Lys His Leu Val Ile Lys 165 170 175 Asp Ser Lys Leu Asn Asn Thr Asn Ile Arg Asn Ser Glu Lys Val Tyr 180 185 190 Ser Cys Asp Gln Glu Arg Gln Ser Ala Leu Glu Glu Ala Gln Gln Asn 195 200 205 Pro Arg Glu Gly Ile Val Ile Pro Glu Cys Ala Pro Gly Gly Leu Tyr 210 215 220 Lys Pro Val Gln Cys His Gln Ser Thr Gly Tyr Cys Trp Cys Val Leu 225 230 235 240 Val Asp Thr Gly Arg Pro Leu Pro Gly Thr Ser Thr Arg Tyr Val Met 245 250 255 Pro Ser Cys Glu Ser Asp Ala Arg Ala Lys Thr Thr Glu Ala Asp Asp 260 265 270 Pro Phe Lys Asp Arg Glu Leu Pro Gly Cys Pro Glu Gly Lys Lys Met 275 280 285 Glu Phe Ile Thr Ser Leu Leu Asp Ala Leu Thr Thr Asp Met Val Gln 290 295 300 Ala Ile Asn Ser Ala Ala Pro Thr Gly Gly Gly Arg Phe Ser Glu Pro 305 310 315 320 Asp Pro Ser His Thr Leu Glu Glu Arg Val Val His Trp Tyr Phe Ser 325 330 335 Gln Leu Asp Ser Asn Ser Ser Asn Asp Ile Asn Lys Arg Glu Met Lys 340 345 350 Pro Phe Lys Arg Tyr Val Lys Lys Lys Ala Lys Pro Lys Lys Cys Ala 355 360 365 Arg Arg Phe Thr Asp Tyr Cys Asp Leu Asn Lys Asp Lys Val Ile Ser 370 375 380 Leu Pro Glu Leu Lys Gly Cys Leu Gly Val Ser Lys Glu Gly Gly Ser 385 390 395 400 Leu Gly Ser Phe Pro Gln Ala Lys 405 40 434 PRT Homo sapiens 40 Met Ala Gly Ser Gly Pro Pro Leu Pro Thr Cys Asn Ala Glu Val Gly 1 5 10 15 Trp Glu Asn Met Ala Glu Asp Gly Lys Ala Phe Leu Ile Ser Asp Arg 20 25 30 Asp Pro Gln Cys Asn Leu His Cys Ser Arg Thr Gln Pro Lys Pro Ile 35 40 45 Cys Ala Ser Asp Gly Arg Ser Tyr Glu Ser Met Cys Glu Tyr Gln Arg 50 55 60 Ala Lys Cys Arg Asp Pro Thr Leu Gly Val Val His Arg Gly Arg Cys 65 70 75 80 Lys Asp Ala Gly Gln Ser Lys Cys Arg Leu Glu Arg Ala Gln Ala Leu 85 90 95 Glu Gln Ala Lys Lys Pro Gln Glu Ala Val Phe Val Pro Glu Cys Gly 100 105 110 Glu Asp Gly Ser Phe Thr Gln Val Gln Cys His Thr Tyr Thr Gly Tyr 115 120 125 Cys Trp Cys Val Thr Pro Asp Gly Lys Pro Ile Ser Gly Ser Ser Val 130 135 140 Gln Asn Lys Thr Pro Val Cys Ser Gly Ser Val Thr Asp Lys Pro Leu 145 150 155 160 Ser Gln Gly Asn Ser Gly Arg Lys Asp Asp Gly Ser Lys Pro Thr Pro 165 170 175 Thr Met Glu Thr Gln Pro Val Phe Asp Gly Asp Glu Ile Thr Ala Pro 180 185 190 Thr Leu Trp Ile Lys His Leu Val Ile Lys Asp Ser Lys Leu Asn Asn 195 200 205 Thr Asn Ile Arg Asn Ser Glu Lys Val Tyr Ser Cys Asp Gln Glu Arg 210 215 220 Gln Ser Ala Leu Glu Glu Ala Gln Gln Asn Pro Arg Glu Gly Ile Val 225 230 235 240 Ile Pro Glu Cys Ala Pro Gly Gly Leu Tyr Lys Pro Val Gln Cys His 245 250 255 Gln Ser Thr Gly Tyr Cys Trp Cys Val Leu Val Asp Thr Gly Arg Pro 260 265 270 Leu Pro Gly Thr Ser Thr Arg Tyr Val Met Pro Ser Cys Glu Ser Asp 275 280 285 Ala Arg Ala Lys Thr Thr Glu Ala Asp Asp Pro Phe Lys Asp Arg Glu 290 295 300 Leu Pro Gly Cys Pro Glu Gly Lys Lys Met Glu Phe Ile Thr Ser Leu 305 310 315 320 Leu Asp Ala Leu Thr Thr Asp Met Val Gln Ala Ile Asn Ser Ala Ala 325 330 335 Pro Thr Gly Gly Gly Arg Phe Ser Glu Pro Asp Pro Ser His Thr Leu 340 345 350 Glu Glu Arg Val Val His Trp Tyr Phe Ser Gln Leu Asp Ser Asn Ser 355 360 365 Ser Asn Asp Ile Asn Lys Arg Glu Met Lys Pro Phe Lys Arg Tyr Val 370 375 380 Lys Lys Lys Ala Lys Pro Lys Lys Cys Ala Arg Arg Phe Thr Asp Tyr 385 390 395 400 Cys Asp Leu Asn Lys Asp Lys Val Ile Ser Leu Pro Glu Leu Lys Gly 405 410 415 Cys Leu Gly Val Ser Lys Glu Gly Gly Ser Leu Gly Ser Phe Pro Gln 420 425 430 Ala Lys 41 250 PRT Homo sapiens 41 Met Ala Cys Trp Trp Pro Leu Leu Leu Glu Leu Trp Thr Val Met Pro 1 5 10 15 Thr Trp Ala Gly Asp Glu Leu Leu Asn Ile Cys Met Asn Ala Lys His 20 25 30 His Lys Arg Val Pro Ser Pro Glu Asp Lys Leu Tyr Glu Glu Cys Ile 35 40 45 Pro Trp Lys Asp Asn Ala Cys Cys Thr Leu Thr Thr Ser Trp Glu Ala 50 55 60 His Leu Asp Val Ser Pro Leu Tyr Asn Phe Ser Leu Phe His Cys Gly 65 70 75 80 Leu Leu Met Pro Gly Cys Arg Lys His Phe Ile Gln Ala Ile Cys Phe 85 90 95 Tyr Glu Cys Ser Pro Asn Leu Gly Pro Trp Ile Gln Pro Val Gly Ser 100 105 110 Leu Gly Trp Glu Val Ala Pro Ser Gly Gln Gly Glu Arg Val Val Asn 115 120 125 Val Pro Leu Cys Gln Glu Asp Cys Glu Glu Trp Trp Glu Asp Cys Arg 130 135 140 Met Ser Tyr Thr Cys Lys Ser Asn Trp Arg Gly Gly Trp Asp Trp Ser 145 150 155 160 Gln Gly Lys Asn Arg Cys Pro Lys Gly Ala Gln Cys Leu Pro Phe Ser 165 170 175 His Tyr Phe Pro Thr Pro Ala Asp Leu Cys Glu Lys Thr Trp Ser Asn 180 185 190 Ser Phe Lys Ala Ser Pro Glu Arg Arg Asn Ser Gly Arg Cys Leu Gln 195 200 205 Lys Trp Phe Glu Pro Ala Gln Gly Asn Pro Asn Val Ala Val Ala Arg 210 215 220 Leu Phe Ala Ser Ser Ala Pro Ser Trp Glu Leu Ser Tyr Thr Ile Met 225 230 235 240 Val Cys Ser Leu Phe Leu Pro Phe Leu Ser 245 250 42 257 PRT Homo sapiens 42 Met Gly Thr Val Arg Pro Pro Arg Pro Ser Leu Leu Leu Val Ser Thr 1 5 10 15 Arg Glu Ser Cys Leu Phe Leu Leu Phe Cys Leu His Leu Gly Ala Ala 20 25 30 Cys Pro Gln Pro Cys Arg Cys Pro Asp His Ala Gly Ala Val Ala Val 35 40 45 Phe Cys Ser Leu Arg Gly Leu Gln Glu Val Pro Glu Asp Ile Pro Ala 50 55 60 Asn Thr Val Leu Leu Lys Leu Asp Ala Asn Lys Ile Ser His Leu Pro 65 70 75 80 Asp Gly Ala Phe Gln His Leu His Arg Leu Arg Glu Leu Asp Leu Ser 85 90 95 His Asn Ala Ile Glu Ala Ile Gly Ser Ala Thr Phe Ala Gly Leu Ala 100 105 110 Gly Gly Leu Arg Leu Leu Asp Leu Ser Tyr Asn Arg Ile Gln Arg Ile 115 120 125 Pro Lys Asp Ala Leu Gly Lys Leu Ser Ala Lys Ile Arg Leu Ser His 130 135 140 Asn Pro Leu His Cys Glu Cys Ala Leu Gln Glu Ala Leu Trp Glu Leu 145 150 155 160 Lys Leu Asp Pro Asp Ser Val Asp Glu Ile Ala Cys His Thr Ser Val 165 170 175 Gln Glu Glu Phe Val Gly Lys Pro Leu Val Gln Ala Leu Asp Ala Gly 180 185 190 Ala Ser Leu Cys Ser Val Pro His Arg Thr Thr Asp Val Ala Met Leu 195 200 205 Val Thr Met Phe Gly Trp Phe Ala Met Val Ile Ala Tyr Val Val Tyr 210 215 220 Tyr Val Arg His Asn Gln Glu Asp Ala Arg Arg His Leu Glu Tyr Leu 225 230 235 240 Lys Ser Leu Pro Ser Ala Pro Ala Ser Lys Asp Pro Ile Gly Pro Gly 245 250 255 Pro 43 148 PRT Homo sapiens 43 Met Leu Gly Leu Pro Trp Lys Gly Gly Leu Ser Trp Ala Leu Leu Leu 1 5 10 15 Leu Leu Leu Gly Ser Gln Ile Leu Leu Ile Tyr Ala Trp His Phe His 20 25 30 Glu Gln Arg Asp Cys Asp Glu His Asn Val Met Ala Arg Tyr Leu Pro 35 40 45 Ala Thr Val Glu Phe Ala Val His Thr Phe Asn Gln Gln Ser Lys Asp 50 55 60 Tyr Tyr Ala Tyr Arg Leu Gly His Ile Leu Asn Ser Trp Lys Glu Gln 65 70 75 80 Val Glu Ser Lys Thr Val Phe Ser Met Glu Leu Leu Leu Gly Arg Thr 85 90 95 Arg Cys Gly Lys Phe Glu Asp Asp Ile Asp Asn Cys His Phe Gln Glu 100 105 110 Ser Thr Glu Leu Asn Asn Val Arg Gln Asp Thr Ser Phe Pro Pro Gly 115 120 125 Tyr Ser Cys Gly Cys His Met Gly Cys Gly Val Gly Thr Gly Ala Thr 130 135 140 Asp Lys Glu Thr 145 44 355 PRT Homo sapiens 44 Met Gly Pro Lys Asp Ser Ala Lys Cys Leu His Arg Gly Pro Gln Pro 1 5 10 15 Ser His Trp Ala Ala Gly Asp Gly Pro Thr Gln Glu Arg Cys Gly Pro 20 25 30 Arg Ser Leu Gly Ser Pro Val Leu Gly Leu Asp Thr Cys Arg Ala Trp 35 40 45 Asp His Val Asp Gly Gln Ile Leu Gly Gln Leu Arg Pro Leu Thr Glu 50 55 60 Glu Glu Glu Glu Glu Gly Ala Gly Ala Thr Leu Ser Arg Gly Pro Ala 65 70 75 80 Phe Pro Gly Met Gly Ser Glu Glu Leu Arg Leu Ala Ser Phe Tyr Asp 85 90 95 Trp Pro Leu Thr Ala Glu Val Pro Pro Glu Leu Leu Ala Ala Ala Gly 100 105 110 Phe Phe His Thr Gly His Gln Asp Lys Val Arg Cys Phe Phe Cys Tyr 115 120 125 Gly Gly Leu Gln Ser Trp Lys Arg Gly Asp Asp Pro Trp Thr Glu His 130 135 140 Ala Lys Trp Phe Pro Ser Cys Gln Phe Leu Leu Arg Ser Lys Gly Arg 145 150 155 160 Asp Phe Val His Ser Val Gln Glu Thr His Ser Gln Leu Leu Gly Ser 165 170 175 Trp Val Ser Ala Thr Ser Pro Arg Gly Ser Gly Trp Gln Trp Gly Pro 180 185 190 Ala Pro Pro Ile Ser Pro Arg Pro Asp Gly Leu Trp Leu Leu Pro Gly 195 200 205 Pro Val Gly Arg Thr Gly Arg Arg Ser Pro Cys Gly Pro Leu Arg Ser 210 215 220 Ser Leu Lys Val Pro Arg Ser Gln Val Gln Ala Arg Asp Pro Leu Gly 225 230 235 240 Glu Gly Trp Gly Arg Gly Gly Leu Arg Asp Pro Asp Leu Pro Trp Pro 245 250 255 Ile Glu Gly Gly Gly Gln Gly Val Gly Thr Phe Arg Arg Pro Val Leu 260 265 270 Leu Gly Gly Val Ser Pro Ala Glu Ala Gln Arg Ala Trp Trp Val Leu 275 280 285 Glu Pro Pro Gly Ala Arg Asp Val Glu Ala Gln Leu Arg Arg Leu Gln 290 295 300 Glu Glu Arg Thr Cys Lys Val Cys Leu Asp Arg Ala Val Ser Ile Val 305 310 315 320 Phe Val Pro Cys Gly His Leu Val Cys Ala Glu Cys Ala Pro Gly Leu 325 330 335 Gln Leu Cys Pro Ile Cys Arg Ala Pro Val Arg Ser Arg Val Arg Thr 340 345 350 Phe Leu Ser 355 45 255 PRT Homo sapiens 45 Met Gly Pro Lys Asp Ser Ala Lys Cys Leu His Arg Gly Pro Gln Pro 1 5 10 15 Ser His Trp Ala Ala Gly Asp Gly Pro Thr Gln Glu Arg Cys Gly Pro 20 25 30 Arg Ser Leu Gly Ser Pro Val Leu Gly Leu Asp Thr Cys Arg Ala Trp 35 40 45 Asp His Val Asp Gly Gln Ile Leu Gly Gln Leu Arg Pro Leu Thr Glu 50 55 60 Glu Glu Glu Glu Glu Gly Ala Gly Ala Thr Leu Ser Arg Gly Pro Ala 65 70 75 80 Phe Pro Gly Met Gly Ser Glu Glu Leu Arg Leu Ala Ser Phe Tyr Asp 85 90 95 Trp Pro Leu Thr Ala Glu Val Pro Pro Glu Leu Leu Ala Ala Ala Gly 100 105 110 Phe Phe His Thr Gly His Gln Asp Lys Val Arg Cys Phe Phe Cys Tyr 115 120 125 Gly Gly Leu Gln Ser Trp Lys Arg Gly Asp Asp Pro Trp Thr Glu His 130 135 140 Ala Lys Trp Phe Pro Leu Ser Val Pro Ala Pro Val Lys Arg Lys Arg 145 150 155 160 Leu Cys Pro Gln Cys Ala Gly Asp Ser Leu Pro Ala Ala Gly Leu Leu 165 170 175 Gly Pro Val Gly Arg Thr Gly Arg Arg Ser Pro Cys Gly Pro Leu Arg 180 185 190 Ser Gln Gly Cys Gly Gly Ala Ala Ala Ala Ala Ala Gly Gly Glu Asp 195 200 205 Val Gln Gly Val Pro Gly Pro Arg Arg Val His Arg Leu Cys Ala Val 210 215 220 Arg Pro Pro Gly Leu Cys Val Cys Pro Arg Pro Ala Ala Val Pro His 225 230 235 240 Leu Gln Ser Pro Arg Pro Gln Pro Arg Ala His Leu Pro Val Leu 245 250 255 46 251 PRT Homo sapiens 46 Met Leu Gly Ala Arg Leu Arg Leu Trp Val Cys Ala Leu Cys Ser Val 1 5 10 15 Cys Ser Met Ser Val Leu Arg Ala Tyr Pro Asn Ala Ser Pro Leu Leu 20 25 30 Gly Ser Ser Trp Gly Gly Leu Ile His Leu Tyr Thr Ala Thr Ala Arg 35 40 45 Asn Ser Tyr His Leu Gln Ile His Lys Asn Gly His Val Asp Gly Ala 50 55 60 Pro His Gln Thr Ile Tyr Ser Ala Leu Met Ile Arg Ser Glu Asp Ala 65 70 75 80 Gly Phe Val Val Ile Thr Gly Val Met Ser Arg Arg Tyr Leu Cys Met 85 90 95 Asp Phe Arg Gly Asn Ile Phe Gly Ser His Tyr Phe Asp Pro Glu Asn 100 105 110 Cys Arg Phe Gln His Gln Thr Leu Glu Asn Gly Tyr Asp Val Tyr His 115 120 125 Ser Pro Gln Tyr His Phe Leu Val Ser Leu Gly Arg Ala Lys Arg Ala 130 135 140 Phe Leu Pro Gly Met Asn Pro Pro Pro Tyr Ser Gln Phe Leu Ser Arg 145 150 155 160 Arg Asn Glu Ile Pro Leu Ile His Phe Asn Thr Pro Ile Pro Arg Arg 165 170 175 His Thr Arg Ser Ala Glu Asp Asp Ser Glu Arg Asp Pro Leu Asn Val 180 185 190 Leu Lys Pro Arg Ala Arg Met Thr Pro Ala Pro Ala Ser Cys Ser Gln 195 200 205 Glu Leu Pro Ser Ala Glu Asp Asn Ser Pro Met Ala Ser Asp Pro Leu 210 215 220 Gly Val Val Arg Gly Gly Arg Val Asn Thr His Ala Gly Gly Thr Gly 225 230 235 240 Pro Glu Gly Cys Arg Pro Phe Ala Lys Phe Ile 245 250 

What is claimed is:
 1. An isolated polypeptide selected from the group consisting of: (a) an isolated polypeptide encoded by a polynucleotide comprising a sequence set forth in Table I; (b) an isolated polypeptide comprising a polypeptide sequence having at least 95% identity to a polypeptide sequence set forth in Table I; (c) an isolated polypeptide comprising a polypeptide sequence set forth in Table I; (d) an isolated polypeptide having at least 95% identity to a polypeptide sequence set forth in Table I; (e) a polypeptide sequence of a gene set forth in Table I; and (f) fragments and variants of such polypeptides in (a) to (e)
 2. An isolated polynucleotide selected from the group consisting of: (a) an isolated polynucleotide comprising a polynucleotide sequence having at least 95% identity to a polynucleotide sequence set forth in Table I; (b) an isolated polynucleotide comprising a polynucleotide set forth in Table I; (c) an isolated polynucleotide having at least 95% identity to a polynucleotide set forth in Table I; (d) an isolated polynucleotide of a gene set forth in Table I; (e) an isolated polynucleotide comprising a polynucleotide sequence encoding a polypeptide sequence having at least 95% identity to the polypeptide sequence set forth in Table I; (f) an isolated polynucleotide comprising a polynucleotide sequence encoding a polypeptide set forth in Table I; (g) an isolated polynucleotide having a polynucleotide sequence encoding a polypeptide sequence having at least 95% identity to a polypeptide sequence set forth in Table I; (h) an isolated polynucleotide encoding a polypeptide set forth in Table I; (i) an isolated polynucleotide with a nucleotide sequence of at least 100 nucleotides obtained by screening a library under stringent hybridization conditions with a labelled probe having a sequence set forth in Table I or a fragment thereof having at least 15 nucleotides; (j) a polynucleotide which is an RNA equivalent of the polynucleotide of (a) to (i); or a polynucleotide sequence complementary to said isolated polynucleotide and polynucleotides that are variants and fragments of the above mentioned polynucleotides or that are complementary to above mentioned polynucleotides, over the entire length thereof.
 3. An antibody immunospecific for the polypeptide of claim
 1. 4. An antibody as claimed in claim 3 which is a polyclonal antibody.
 5. An expression vector comprising a polynucleotide capable of producing a polypeptide of claim 1 when said expression vector is present in a compatible host cell.
 6. A process for producing a recombinant host cell which comprises the step of introducing an expression vector comprising a polynucleotide capable of producing a polypeptide of claim 1 into a cell such that the host cell, under appropriate culture conditions, produces said polypeptide.
 7. A recombinant host cell produced by the process of claim
 6. 8. A membrane of a recombinant host cell of claim 7 expressing said polypeptide.
 9. A process for producing a polypeptide which comprises culturing a host cell of claim 7 under conditions sufficient for the production of said polypeptide and recovering said polypeptide from the culture. 